A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503595



Internal ID18801876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45435633..45465681hg38UCSC Ensembl
Innerchr11:45457183..45487231hg19UCSC Ensembl
Innerchr11:45413759..45443807hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3830049
hg1930049
hg1830049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035254
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)nssv3503595
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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