A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523860



Internal ID18822141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54773815..54832407hg38UCSC Ensembl
Innerchr13:55347950..55406542hg19UCSC Ensembl
Innerchr13:54245951..54304543hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3858593
hg1958593
hg1858593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053550
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)nssv3523860
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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