A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768279



Internal ID15715549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16198743..16286154hg38UCSC Ensembl
Innerchr11:16220289..16307700hg19UCSC Ensembl
Innerchr11:16176865..16264276hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3887412
hg1987412
hg1887412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553565
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)nssv768279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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