U.S. flag

An official website of the United States government

nsv5526841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:151

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 27 studies. See in: genome view    
Submitted genomic67,175,987-67,176,137Question Mark
Overlapping variant regions from other studies: 130 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):67,209,890-67,210,040Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,175,98767,176,137
nsv5526841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,209,89067,210,040

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707484deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707484Submitted genomicNC_000016.10:g.671
75987_67176137del
GRCh38 (hg38)NC_000016.10Chr1667,175,98767,176,137
nssv17707484RemappedPerfectNC_000016.9:g.6720
9890_67210040del
GRCh37.p13First PassNC_000016.9Chr1667,209,89067,210,040

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)
nssv17707484<0.00126404
Support Center