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nsv4526449

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:270,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 195 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):68,494,083-68,764,084Question Mark
Overlapping variant regions from other studies: 195 SVs from 17 studies. See in: genome view    
Submitted genomic71,108,999-71,379,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4526449RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr968,494,08368,764,084
nsv4526449Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr971,108,99971,379,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15986312duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15986312RemappedPerfectNC_000009.12:g.684
94083_68764084dup
GRCh38.p12First PassNC_000009.12Chr968,494,08368,764,084
nssv15986312Submitted genomicNC_000009.11:g.711
08999_71379000dup
GRCh37.p13NC_000009.11Chr971,108,99971,379,000

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)
nssv159863124.6e-005121694
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