A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710061



Internal ID19008342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23774916..23848745hg38UCSC Ensembl
Innerchr11:23796462..23870291hg19UCSC Ensembl
Innerchr11:23753038..23826867hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3873830
hg1973830
hg1873830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710061
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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