A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519579



Internal ID15446872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51531920..51556118hg38UCSC Ensembl
Innerchr17:49609281..49633479hg19UCSC Ensembl
Innerchr17:46964280..46988478hg18UCSC Ensembl
Innerchr17:46964280..46988478hg17UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3824199
hg1924199
hg1824199
hg1724199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696932
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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