A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510546



Internal ID18808827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119901039..119938155hg38UCSC Ensembl
Innerchr11:119771748..119808864hg19UCSC Ensembl
Innerchr11:119276958..119314074hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837117
hg1937117
hg1837117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048084
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)nssv3510546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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