A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511400



Internal ID18809681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134973916..135074876hg38UCSC Ensembl
Innerchr11:134843810..134944770hg19UCSC Ensembl
Innerchr11:134349020..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38100961
hg19100961
hg18100963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049414
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)nssv3511400
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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