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nsv5534769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 19 studies. See in: genome view    
Submitted genomic46,738,749-46,738,784Question Mark
Overlapping variant regions from other studies: 119 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):46,965,888-46,965,923Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr246,738,74946,738,784
nsv5534769RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr246,965,88846,965,923

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913667insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913667Submitted genomicNC_000002.12:g.467
38749_46738784ins3
20
GRCh38 (hg38)NC_000002.12Chr246,738,74946,738,784
nssv16913667RemappedPerfectNC_000002.11:g.469
65888_46965923ins3
20
GRCh37.p13First PassNC_000002.11Chr246,965,88846,965,923

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)
nssv16913667<0.00146404
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