A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519000



Internal ID18470595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58786043..58911023hg38UCSC Ensembl
Innerchr11:58553516..58678496hg19UCSC Ensembl
Innerchr11:58310092..58435072hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38124981
hg19124981
hg18124981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052173
Supporting Variants
Samples
Known GenesGLYATL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519000
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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