A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508200



Internal ID18806481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96895663..96943720hg38UCSC Ensembl
Innerchr11:96766663..96814720hg19UCSC Ensembl
Innerchr11:96271873..96319930hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3848058
hg1948058
hg1848058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045401
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)nssv3508200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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