A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174796



Internal ID15853526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55937346..55962275hg38UCSC Ensembl
Innerchr11:55704822..55729751hg19UCSC Ensembl
Innerchr11:55461398..55486327hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3824930
hg1924930
hg1824930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555090
Supporting Variants
Samples1780854261_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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