A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515651



Internal ID15443262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31756668..31772603hg38UCSC Ensembl
Innerchr17:30083687..30099622hg19UCSC Ensembl
Innerchr17:27107800..27123735hg18UCSC Ensembl
Innerchr17:27107800..27123735hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3815936
hg1915936
hg1815936
hg1715936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681526, nssv658670, nssv664252
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515651
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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