A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524625



Internal ID15105232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12431197..12431494hg38UCSC Ensembl
Innerchr11:12452744..12453041hg19UCSC Ensembl
Innerchr11:12409320..12409617hg18UCSC Ensembl
Innerchr11:12409320..12409617hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38298
hg19298
hg18298
hg17298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700587
Samples
Known GenesPARVA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524625
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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