A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526555



Internal ID15107162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33847061..33864748hg38UCSC Ensembl
Innerchr11:33868607..33886294hg19UCSC Ensembl
Innerchr11:33825183..33842870hg18UCSC Ensembl
Innerchr11:33825183..33842870hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3817688
hg1917688
hg1817688
hg1717688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702869
Samples
Known GenesLMO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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