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nsv5479121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,799

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 23 studies. See in: genome view    
Submitted genomic63,784,958-63,786,756Question Mark
Overlapping variant regions from other studies: 114 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):64,697,515-64,699,313Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr863,784,95863,786,756
nsv5479121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr864,697,51564,699,313

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17012623deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17012623Submitted genomicNC_000008.11:g.637
84958_63786756del
GRCh38 (hg38)NC_000008.11Chr863,784,95863,786,756
nssv17012623RemappedPerfectNC_000008.10:g.646
97515_64699313del
GRCh37.p13First PassNC_000008.10Chr864,697,51564,699,313

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)
nssv17012623<0.00126404
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