A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175393



Internal ID15853837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91222804..91265428hg38UCSC Ensembl
Innerchr11:90955972..90998596hg19UCSC Ensembl
Innerchr11:90595620..90638244hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3842625
hg1942625
hg1842625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555895
Supporting Variants
Samples1780854459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175393
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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