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nsv4234127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:732

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 69 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):3,666,590-3,667,321Question Mark
Overlapping variant regions from other studies: 69 SVs from 6 studies. See in: genome view    
Submitted genomic3,569,884-3,570,615Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4234127RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr173,666,5903,667,321
nsv4234127Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr173,569,8843,570,615

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15832963deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15832963RemappedPerfectNC_000017.11:g.366
6590_3667321del
GRCh38.p12First PassNC_000017.11Chr173,666,5903,667,321
nssv15832963Submitted genomicNC_000017.10:g.356
9884_3570615del
GRCh37.p13NC_000017.10Chr173,569,8843,570,615

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)
nssv158329634.6e-005121694
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