A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699015



Internal ID15435667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24756913..24765107hg38UCSC Ensembl
Innerchr11:24778459..24786653hg19UCSC Ensembl
Innerchr11:24735035..24743229hg18UCSC Ensembl
Innerchr11:24735035..24743229hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg388195
hg198195
hg188195
hg178195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523280
Supporting Variants
Samples
Known GenesLUZP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699015
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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