A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511726



Internal ID18810007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37746263..37826023hg38UCSC Ensembl
Innerchr11:37767813..37847573hg19UCSC Ensembl
Innerchr11:37724389..37804149hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3879761
hg1979761
hg1879761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040071
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)nssv3511726
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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