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nsv7098707

  • Variant Calls:6
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):17,955,071-17,955,071Question Mark
    Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):17,955,072-17,955,072Question Mark
    Overlapping variant regions from other studies: 103 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):55,757,575-55,757,575Question Mark
    Overlapping variant regions from other studies: 103 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):55,757,575-55,757,575Question Mark
    Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):109,330,068-109,330,068Question Mark
    Overlapping variant regions from other studies: 159 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):115,924,901-115,924,901Question Mark
    Overlapping variant regions from other studies: 359 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):77,013,041-77,013,041Question Mark
    Overlapping variant regions from other studies: 359 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):77,013,041-77,013,041Question Mark
    Overlapping variant regions from other studies: 429 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):79,484,456-79,484,456Question Mark
    Overlapping variant regions from other studies: 429 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):79,484,456-79,484,456Question Mark
    Overlapping variant regions from other studies: 184 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):18,818,771-18,818,771Question Mark
    Overlapping variant regions from other studies: 184 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):18,818,773-18,818,773Question Mark
    Overlapping variant regions from other studies: 6 SVs from 5 studies. See in: genome view    
    Remapped(Score: Perfect):83,764-83,764Question Mark
    Overlapping variant regions from other studies: 6 SVs from 5 studies. See in: genome view    
    Remapped(Score: Perfect):83,764-83,764Question Mark
    Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
    Submitted genomic17,956,694-17,956,694Question Mark
    Overlapping variant regions from other studies: 119 SVs from 16 studies. See in: genome view    
    Submitted genomic17,956,695-17,956,695Question Mark
    Overlapping variant regions from other studies: 103 SVs from 31 studies. See in: genome view    
    Submitted genomic56,623,741-56,623,741Question Mark
    Overlapping variant regions from other studies: 103 SVs from 31 studies. See in: genome view    
    Submitted genomic56,623,741-56,623,741Question Mark
    Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
    Submitted genomic108,665,769-108,665,769Question Mark
    Overlapping variant regions from other studies: 159 SVs from 29 studies. See in: genome view    
    Submitted genomic115,260,598-115,260,598Question Mark
    Overlapping variant regions from other studies: 359 SVs from 26 studies. See in: genome view    
    Submitted genomic74,724,997-74,724,997Question Mark
    Overlapping variant regions from other studies: 359 SVs from 26 studies. See in: genome view    
    Submitted genomic74,724,997-74,724,997Question Mark
    Overlapping variant regions from other studies: 429 SVs from 38 studies. See in: genome view    
    Submitted genomic77,244,456-77,244,456Question Mark
    Overlapping variant regions from other studies: 429 SVs from 38 studies. See in: genome view    
    Submitted genomic77,244,456-77,244,456Question Mark
    Overlapping variant regions from other studies: 184 SVs from 24 studies. See in: genome view    
    Submitted genomic20,191,089-20,191,089Question Mark
    Overlapping variant regions from other studies: 184 SVs from 24 studies. See in: genome view    
    Submitted genomic20,191,091-20,191,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr417,955,07117,955,071+
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr417,955,07217,955,072-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr455,757,57555,757,575+
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr455,757,57555,757,575-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5109,330,068109,330,068+
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5115,924,901115,924,901-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1877,013,04177,013,041+
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1877,013,04177,013,041-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1879,484,45679,484,456+
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1879,484,45679,484,456-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000021.9Chr2118,818,77118,818,771-
    nsv7098707RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000021.9Chr2118,818,77318,818,773+
    nsv7098707RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187541.1Chr4|NT_18
    7541.1    		83,76483,764+
    nsv7098707RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187541.1Chr4|NT_18
    7541.1    		83,76483,764-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr417,956,69417,956,694+
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr417,956,69517,956,695-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr456,623,74156,623,741+
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr456,623,74156,623,741-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5108,665,769108,665,769+
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5115,260,598115,260,598-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1874,724,99774,724,997+
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1874,724,99774,724,997-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1877,244,45677,244,456+
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1877,244,45677,244,456-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000021.8Chr2120,191,08920,191,089-
    nsv7098707Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000021.8Chr2120,191,09120,191,091+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792435intrachromosomal translocationFHU15-242SequencingSequence alignment6
    nssv18792436interchromosomal translocationFHU15-242SequencingSequence alignment6
    nssv18792440interchromosomal translocationFHU15-242SequencingSequence alignment6
    nssv18792438intrachromosomal translocationFHU15-242SequencingSequence alignment6
    nssv18792437intrachromosomal translocationFHU15-242SequencingSequence alignment6
    nssv18792439interchromosomal translocationFHU15-242SequencingSequence alignment6

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792435RemappedPerfectGRCh38.p12Second PassNT_187541.1Chr4|NT_18
    7541.1    		83,76483,764-
    nssv18792436RemappedPerfectGRCh38.p12Second PassNT_187541.1Chr4|NT_18
    7541.1    		83,76483,764+
    nssv18792440RemappedPerfectGRCh38.p12First PassNC_000004.12Chr417,955,07117,955,071+
    nssv18792435RemappedPerfectGRCh38.p12First PassNC_000004.12Chr417,955,07217,955,072-
    nssv18792435RemappedPerfectGRCh38.p12First PassNC_000004.12Chr455,757,57555,757,575-
    nssv18792436RemappedPerfectGRCh38.p12First PassNC_000004.12Chr455,757,57555,757,575+
    nssv18792438RemappedPerfectGRCh38.p12First PassNC_000005.10Chr5109,330,068109,330,068+
    nssv18792438RemappedPerfectGRCh38.p12First PassNC_000005.10Chr5115,924,901115,924,901-
    nssv18792437RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1877,013,04177,013,041-
    nssv18792439RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1877,013,04177,013,041+
    nssv18792436RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1879,484,45679,484,456+
    nssv18792437RemappedPerfectGRCh38.p12First PassNC_000018.10Chr1879,484,45679,484,456-
    nssv18792439RemappedPerfectGRCh38.p12First PassNC_000021.9Chr2118,818,77118,818,771-
    nssv18792440RemappedPerfectGRCh38.p12First PassNC_000021.9Chr2118,818,77318,818,773+
    nssv18792440Submitted genomicGRCh37 (hg19)NC_000004.11Chr417,956,69417,956,694+
    nssv18792435Submitted genomicGRCh37 (hg19)NC_000004.11Chr417,956,69517,956,695-
    nssv18792435Submitted genomicGRCh37 (hg19)NC_000004.11Chr456,623,74156,623,741-
    nssv18792436Submitted genomicGRCh37 (hg19)NC_000004.11Chr456,623,74156,623,741+
    nssv18792438Submitted genomicGRCh37 (hg19)NC_000005.9Chr5108,665,769108,665,769+
    nssv18792438Submitted genomicGRCh37 (hg19)NC_000005.9Chr5115,260,598115,260,598-
    nssv18792437Submitted genomicGRCh37 (hg19)NC_000018.9Chr1874,724,99774,724,997-
    nssv18792439Submitted genomicGRCh37 (hg19)NC_000018.9Chr1874,724,99774,724,997+
    nssv18792436Submitted genomicGRCh37 (hg19)NC_000018.9Chr1877,244,45677,244,456+
    nssv18792437Submitted genomicGRCh37 (hg19)NC_000018.9Chr1877,244,45677,244,456-
    nssv18792439Submitted genomicGRCh37 (hg19)NC_000021.8Chr2120,191,08920,191,089-
    nssv18792440Submitted genomicGRCh37 (hg19)NC_000021.8Chr2120,191,09120,191,091+

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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