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nsv5455102

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,092

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 19 studies. See in: genome view    
Submitted genomic173,130,873-173,131,964Question Mark
Overlapping variant regions from other studies: 72 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):172,557,876-172,558,967Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5455102Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5173,130,873173,131,964
nsv5455102RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5172,557,876172,558,967

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978658duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978658Submitted genomicNC_000005.10:g.173
130873_173131964du
p
GRCh38 (hg38)NC_000005.10Chr5173,130,873173,131,964
nssv16978658RemappedPerfectNC_000005.9:g.1725
57876_172558967dup
GRCh37.p13First PassNC_000005.9Chr5172,557,876172,558,967

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)
nssv169786580.002116394
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