A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525962



Internal ID15453255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42102899..42117753hg38UCSC Ensembl
Innerchr11:42124449..42139303hg19UCSC Ensembl
Innerchr11:42081025..42095879hg18UCSC Ensembl
Innerchr11:42081025..42095879hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814855
hg1914855
hg1814855
hg1714855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702173
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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