A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768278



Internal ID15715548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16185112..16237859hg38UCSC Ensembl
Innerchr11:16206658..16259405hg19UCSC Ensembl
Innerchr11:16163234..16215981hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3852748
hg1952748
hg1852748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553563
Supporting Variants
Samples
Known GenesSOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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