A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763570



Internal ID15710840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:828784..831809hg38UCSC Ensembl
Innerchr11:828784..831809hg19UCSC Ensembl
Innerchr11:818784..821809hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383026
hg193026
hg183026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552875
Supporting Variants
Samples
Known GenesEFCAB4A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763570
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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