A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519363



Internal ID15446656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21602321..21658650hg38UCSC Ensembl
Innerchr6:21602552..21658881hg19UCSC Ensembl
Innerchr6:21710531..21766860hg18UCSC Ensembl
Innerchr6:21710531..21766860hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3856330
hg1956330
hg1856330
hg1756330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687783, nssv686028, nssv686342, nssv672668, nssv679132, nssv660480, nssv655654, nssv691826, nssv680309, nssv661477
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519363
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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