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nsv5470095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,552

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 33 studies. See in: genome view    
Submitted genomic173,070,065-173,074,616Question Mark
Overlapping variant regions from other studies: 105 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):172,497,068-172,501,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5173,070,065173,074,616
nsv5470095RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5172,497,068172,501,619

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16978651deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16978651Submitted genomicNC_000005.10:g.173
070065_173074616de
l
GRCh38 (hg38)NC_000005.10Chr5173,070,065173,074,616
nssv16978651RemappedPerfectNC_000005.9:g.1724
97068_172501619del
GRCh37.p13First PassNC_000005.9Chr5172,497,068172,501,619

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)
nssv16978651<0.00116404
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