A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526563



Internal ID15453856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79891379..79897744hg38UCSC Ensembl
Innerchr17:77865178..77871543hg19UCSC Ensembl
Innerchr17:75479773..75486138hg18UCSC Ensembl
Innerchr17:75479773..75486138hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386366
hg196366
hg186366
hg176366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv183n21
Supporting Variantsnssv702879
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526563
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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