A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046773



Internal ID18789304
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 StatusM
Merged Variants
Supporting Variantsnssv3509236
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)nsv1046773
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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