A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778758



Internal ID16072714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69450470..69463207hg38UCSC Ensembl
Innerchr11:69265238..69277975hg19UCSC Ensembl
Innerchr11:68974419..68987156hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3812738
hg1912738
hg1812738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555320
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778758
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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