A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520359



Internal ID15100966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78782658..78788699hg38UCSC Ensembl
Innerchr17:76778740..76784781hg19UCSC Ensembl
Innerchr17:74290335..74296376hg18UCSC Ensembl
Innerchr17:74290335..74296376hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386042
hg196042
hg186042
hg176042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697371
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520359
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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