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nsv4063885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):24,074,130-24,079,130Question Mark
Overlapping variant regions from other studies: 27 SVs from 5 studies. See in: genome view    
Submitted genomic24,297,000-24,302,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4063885RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr224,074,13024,079,130
nsv4063885Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr224,297,00024,302,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15967789duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15967789RemappedPerfectNC_000002.12:g.240
74130_24079130dup
GRCh38.p12First PassNC_000002.12Chr224,074,13024,079,130
nssv15967789Submitted genomicNC_000002.11:g.242
97000_24302000dup
GRCh37.p13NC_000002.11Chr224,297,00024,302,000

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)
nssv15967789<0.001521378
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