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nsv6144717

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,719

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 21 studies. See in: genome view    
Submitted genomic90,142,682-90,153,400Question Mark
Overlapping variant regions from other studies: 78 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):90,209,090-90,219,808Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6144717Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1690,142,68290,153,400
nsv6144717RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1690,209,09090,219,808

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17710586duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17710586Submitted genomicNC_000016.10:g.901
42682_90153400dup
GRCh38 (hg38)NC_000016.10Chr1690,142,68290,153,400
nssv17710586RemappedPerfectNC_000016.9:g.9020
9090_90219808dup
GRCh37.p13First PassNC_000016.9Chr1690,209,09090,219,808

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177105860.1554152686
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