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nsv2781945

  • Variant Calls:4
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):6,126,603-6,126,603Question Mark
Overlapping variant regions from other studies: 82 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):6,126,681-6,126,681Question Mark
Overlapping variant regions from other studies: 78 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):7,712,337-7,712,337Question Mark
Overlapping variant regions from other studies: 78 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):7,712,487-7,712,487Question Mark
Overlapping variant regions from other studies: 171 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):24,496,354-24,496,354Question Mark
Overlapping variant regions from other studies: 171 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):24,496,558-24,496,558Question Mark
Overlapping variant regions from other studies: 172 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):24,532,041-24,532,041Question Mark
Overlapping variant regions from other studies: 172 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):24,532,128-24,532,128Question Mark
Overlapping variant regions from other studies: 82 SVs from 13 studies. See in: genome view    
Submitted genomic6,266,735-6,266,735Question Mark
Overlapping variant regions from other studies: 82 SVs from 13 studies. See in: genome view    
Submitted genomic6,266,813-6,266,813Question Mark
Overlapping variant regions from other studies: 78 SVs from 13 studies. See in: genome view    
Submitted genomic7,852,468-7,852,468Question Mark
Overlapping variant regions from other studies: 78 SVs from 13 studies. See in: genome view    
Submitted genomic7,852,618-7,852,618Question Mark
Overlapping variant regions from other studies: 171 SVs from 31 studies. See in: genome view    
Submitted genomic24,649,288-24,649,288Question Mark
Overlapping variant regions from other studies: 171 SVs from 31 studies. See in: genome view    
Submitted genomic24,649,492-24,649,492Question Mark
Overlapping variant regions from other studies: 172 SVs from 32 studies. See in: genome view    
Submitted genomic24,684,975-24,684,975Question Mark
Overlapping variant regions from other studies: 172 SVs from 32 studies. See in: genome view    
Submitted genomic24,685,062-24,685,062Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr26,126,6036,126,603+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr26,126,6816,126,681+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr27,712,3377,712,337+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr27,712,4877,712,487+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1224,496,35424,496,354+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1224,496,55824,496,558+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1224,532,04124,532,041+
nsv2781945RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1224,532,12824,532,128+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr26,266,7356,266,735+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr26,266,8136,266,813+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr27,852,4687,852,468+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr27,852,6187,852,618+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1224,649,28824,649,288+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1224,649,49224,649,492+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1224,684,97524,684,975+
nsv2781945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1224,685,06224,685,062+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisClinVar IDOther Calls in this Sample and Study
nssv13660388interchromosomal translocationROC43SequencingSplit read and paired-end mappingSCV000320941nssv13660387, nssv13660401, nssv13660402
nssv13660401interchromosomal translocationROC43SequencingSplit read and paired-end mappingSCV000320941nssv13660387, nssv13660388, nssv13660402
nssv13660402interchromosomal translocationROC43SequencingSplit read and paired-end mappingSCV000320941nssv13660387, nssv13660388, nssv13660401
nssv13660387interchromosomal translocationROC43SequencingSplit read and paired-end mappingSCV000320941nssv13660388, nssv13660401, nssv13660402

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv13660388RemappedPerfectGRCh38.p12First PassNC_000002.12Chr26,126,6036,126,603+
nssv13660401RemappedPerfectGRCh38.p12First PassNC_000002.12Chr26,126,6816,126,681+
nssv13660402RemappedPerfectGRCh38.p12First PassNC_000002.12Chr27,712,3377,712,337+
nssv13660387RemappedPerfectGRCh38.p12First PassNC_000002.12Chr27,712,4877,712,487+
nssv13660401RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1224,496,35424,496,354+
nssv13660402RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1224,496,55824,496,558+
nssv13660387RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1224,532,04124,532,041+
nssv13660388RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1224,532,12824,532,128+
nssv13660388Submitted genomicGRCh37 (hg19)NC_000002.11Chr26,266,7356,266,735+
nssv13660401Submitted genomicGRCh37 (hg19)NC_000002.11Chr26,266,8136,266,813+
nssv13660402Submitted genomicGRCh37 (hg19)NC_000002.11Chr27,852,4687,852,468+
nssv13660387Submitted genomicGRCh37 (hg19)NC_000002.11Chr27,852,6187,852,618+
nssv13660401Submitted genomicGRCh37 (hg19)NC_000012.11Chr1224,649,28824,649,288+
nssv13660402Submitted genomicGRCh37 (hg19)NC_000012.11Chr1224,649,49224,649,492+
nssv13660387Submitted genomicGRCh37 (hg19)NC_000012.11Chr1224,684,97524,684,975+
nssv13660388Submitted genomicGRCh37 (hg19)NC_000012.11Chr1224,685,06224,685,062+

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDSample IDTypeClinical InterpretationClinVar IDGenderOther Calls in this Sample and Study
nssv13660388ROC43interchromosomal translocationSCV000320941Malenssv13660387, nssv13660401, nssv13660402
nssv13660401ROC43interchromosomal translocationSCV000320941Malenssv13660387, nssv13660388, nssv13660402
nssv13660402ROC43interchromosomal translocationSCV000320941Malenssv13660387, nssv13660388, nssv13660401
nssv13660387ROC43interchromosomal translocationSCV000320941Malenssv13660388, nssv13660401, nssv13660402

No genotype data were submitted for this variant

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