A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509236



Internal ID18460831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22597901..23427777hg38UCSC Ensembl
Innerchr11:22619447..23449323hg19UCSC Ensembl
Innerchr11:22576023..23405899hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38829877
hg19829877
hg18829877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046773
Supporting Variants
Samples
Known GenesCCDC179, FANCF, GAS2, MIR8054, SVIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509236
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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