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nsv5489220

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 74 SVs from 17 studies. See in: genome view    
Submitted genomic123,190,805-123,190,938Question Mark
Overlapping variant regions from other studies: 74 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):125,953,084-125,953,217Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489220Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9123,190,805123,190,938
nsv5489220RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,953,084125,953,217

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027156deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027156Submitted genomicNC_000009.12:g.123
190805_123190938de
l
GRCh38 (hg38)NC_000009.12Chr9123,190,805123,190,938
nssv17027156RemappedPerfectNC_000009.11:g.125
953084_125953217de
l
GRCh37.p13First PassNC_000009.11Chr9125,953,084125,953,217

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)
nssv17027156<0.00116404
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