A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520706



Internal ID15447999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76597821..76600882hg38UCSC Ensembl
Innerchr17:74593903..74596964hg19UCSC Ensembl
Innerchr17:72105498..72108559hg18UCSC Ensembl
Innerchr17:72105498..72108559hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383062
hg193062
hg183062
hg173062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694081
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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