U.S. flag

An official website of the United States government

nsv5564080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Submitted genomic66,314,068-66,314,119Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):64,310,186-64,310,237Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1766,314,06866,314,119
nsv5564080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1764,310,18664,310,237

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714141sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714141Submitted genomicNC_000017.11:g.663
14068_66314119ins1
290
GRCh38 (hg38)NC_000017.11Chr1766,314,06866,314,119
nssv17714141RemappedPerfectNC_000017.10:g.643
10186_64310237ins1
290
GRCh37.p13First PassNC_000017.10Chr1764,310,18664,310,237

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)
nssv17714141<0.00116404
Support Center