A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520677



Internal ID18818958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37732365..37804340hg38UCSC Ensembl
Innerchr11:37753915..37825890hg19UCSC Ensembl
Innerchr11:37710491..37782466hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3871976
hg1971976
hg1871976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052864
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)nssv3520677
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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