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nsv5523610

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:114,898

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 427 SVs from 52 studies. See in: genome view    
Submitted genomic27,201,257-27,316,154Question Mark
Overlapping variant regions from other studies: 427 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):27,212,578-27,327,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523610Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1627,201,25727,316,154
nsv5523610RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1627,212,57827,327,475

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706262duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706262Submitted genomicNC_000016.10:g.272
01257_27316154dup
GRCh38 (hg38)NC_000016.10Chr1627,201,25727,316,154
nssv17706262RemappedPerfectNC_000016.9:g.2721
2578_27327475dup
GRCh37.p13First PassNC_000016.9Chr1627,212,57827,327,475

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)
nssv17706262<0.00116404
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