A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523866



Internal ID18822147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55477018..55534294hg38UCSC Ensembl
Innerchr13:56051153..56108429hg19UCSC Ensembl
Innerchr13:54949154..55006430hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3857277
hg1957277
hg1857277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053038
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)nssv3523866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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