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nsv5486893

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:236

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 21 studies. See in: genome view    
Submitted genomic125,205,291-125,205,526Question Mark
Overlapping variant regions from other studies: 83 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):127,967,570-127,967,805Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486893Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9125,205,291125,205,526
nsv5486893RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9127,967,570127,967,805

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028672deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028672Submitted genomicNC_000009.12:g.125
205291_125205526de
l
GRCh38 (hg38)NC_000009.12Chr9125,205,291125,205,526
nssv17028672RemappedPerfectNC_000009.11:g.127
967570_127967805de
l
GRCh37.p13First PassNC_000009.11Chr9127,967,570127,967,805

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)
nssv17028672<0.00116404
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