A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515958



Internal ID18467553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132795918..132836093hg38UCSC Ensembl
Innerchr11:132665813..132705988hg19UCSC Ensembl
Innerchr11:132171023..132211198hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3840176
hg1940176
hg1840176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049431
Supporting Variants
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515958
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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