A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710758



Internal ID19009039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119879626..119905102hg38UCSC Ensembl
Innerchr11:119750335..119775811hg19UCSC Ensembl
Innerchr11:119255545..119281021hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3825477
hg1925477
hg1825477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051526
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)nssv3710758
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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