A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710059



Internal ID19008340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22841980..22872625hg38UCSC Ensembl
Innerchr11:22863526..22894171hg19UCSC Ensembl
Innerchr11:22820102..22850747hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3830646
hg1930646
hg1830646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040326
Supporting Variants
Samples
Known GenesCCDC179
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710059
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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