U.S. flag

An official website of the United States government

nsv5523559

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 314 SVs from 52 studies. See in: genome view    
Submitted genomic36,528,628-36,541,746Question Mark
Overlapping variant regions from other studies: 71 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):413,376-426,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523559Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,528,62836,541,746
nsv5523559RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
03315949.1
413,376426,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712863deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712863Submitted genomicNC_000017.11:g.365
28628_36541746del
GRCh38 (hg38)NC_000017.11Chr1736,528,62836,541,746
nssv17712863RemappedPerfectNW_003315949.1:g.4
13376_426494del
GRCh37.p13First PassNW_003315949.1Chr17|NW_0
03315949.1
413,376426,494

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)
nssv17712863<0.00116404
Support Center