A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564631



Internal ID22433361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170126087..170126087hg38UCSC Ensembl
chr6:170441311..170441311hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331825, nssv14331822, nssv14331824, nssv14331823
SamplesNA19239, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564631
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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