A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773851



Internal ID16067807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48890108..49008635hg38UCSC Ensembl
Innerchr11:48911660..49030187hg19UCSC Ensembl
Innerchr11:48868236..48986763hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38118528
hg19118528
hg18118528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554325
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)nssv773851
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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