A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516326



Internal ID15443619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37666877..37683988hg38UCSC Ensembl
Innerchr11:37688427..37705538hg19UCSC Ensembl
Innerchr11:37645003..37662114hg18UCSC Ensembl
Innerchr11:37645003..37662114hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3817112
hg1917112
hg1817112
hg1717112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690653, nssv673289, nssv687127, nssv688612, nssv660555, nssv656694, nssv667593, nssv688698
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516326
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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