A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773975



Internal ID16067931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50136389..50807137hg38UCSC Ensembl
Innerchr11:50095560..50766308hg19UCSC Ensembl
Innerchr11:50052136..50722884hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38670749
hg19670749
hg18670749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554401
Supporting Variants
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv773975
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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