A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040071



Internal ID19129290
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 StatusM
Merged Variantsdgv1101n100
Supporting Variantsnssv3511726
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)nsv1040071
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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