U.S. flag

An official website of the United States government

nsv5496604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,734

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1987 SVs from 98 studies. See in: genome view    
Submitted genomic19,546,762-19,942,495Question Mark
Overlapping variant regions from other studies: 1987 SVs from 98 studies. See in: genome view    
Remapped(Score: Perfect):20,120,902-20,516,635Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1319,546,76219,942,495
nsv5496604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1320,120,90220,516,635

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17685883duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17685883Submitted genomicNC_000013.11:g.195
46762_19942495dup
GRCh38 (hg38)NC_000013.11Chr1319,546,76219,942,495
nssv17685883RemappedPerfectNC_000013.10:g.201
20902_20516635dup
GRCh37.p13First PassNC_000013.10Chr1320,120,90220,516,635

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)
nssv17685883<0.00116404
Support Center