A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504992



Internal ID18803273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54762047..55021565hg38UCSC Ensembl
Innerchr11:51095992..51357233hg19UCSC Ensembl
Innerchr11:50952568..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38259519
hg19261242
hg18261242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046698
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)nssv3504992
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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