A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524900



Internal ID15452193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120771989..120774502hg38UCSC Ensembl
Innerchr11:120642698..120645211hg19UCSC Ensembl
Innerchr11:120147908..120150421hg18UCSC Ensembl
Innerchr11:120147908..120150421hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382514
hg192514
hg182514
hg172514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700909
Samples
Known GenesGRIK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524900
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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