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nsv5521119

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,945

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 156 SVs from 38 studies. See in: genome view    
Submitted genomic63,914,834-63,918,778Question Mark
Overlapping variant regions from other studies: 156 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):62,546,187-62,550,131Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521119Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,914,83463,918,778
nsv5521119RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2062,546,18762,550,131

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733707deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733707Submitted genomicNC_000020.11:g.639
14834_63918778del
GRCh38 (hg38)NC_000020.11Chr2063,914,83463,918,778
nssv17733707RemappedPerfectNC_000020.10:g.625
46187_62550131del
GRCh37.p13First PassNC_000020.10Chr2062,546,18762,550,131

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)
nssv17733707<0.00136404
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