A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523861



Internal ID18822142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55118815..55144749hg38UCSC Ensembl
Innerchr13:55692950..55718884hg19UCSC Ensembl
Innerchr13:54590951..54616885hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3825935
hg1925935
hg1825935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048283
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)nssv3523861
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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