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nsv4536948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 48 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):41,457,950-41,458,048Question Mark
Overlapping variant regions from other studies: 48 SVs from 7 studies. See in: genome view    
Submitted genomic41,853,954-41,854,052Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4536948RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2241,457,95041,458,048
nsv4536948Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2241,853,95441,854,052

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15865374deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15865374RemappedPerfectNC_000022.11:g.414
57950_41458048del
GRCh38.p12First PassNC_000022.11Chr2241,457,95041,458,048
nssv15865374Submitted genomicNC_000022.10:g.418
53954_41854052del
GRCh37.p13NC_000022.10Chr2241,853,95441,854,052

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)
nssv158653744.6e-005121690
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