A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505786



Internal ID18457381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43925389..43947681hg38UCSC Ensembl
Innerchr11:43946939..43969231hg19UCSC Ensembl
Innerchr11:43903515..43925807hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3822293
hg1922293
hg1822293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039292
Supporting Variants
Samples
Known GenesC11orf96
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505786
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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