A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523864



Internal ID18822145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55294078..55401629hg38UCSC Ensembl
Innerchr13:55868213..55975764hg19UCSC Ensembl
Innerchr13:54766214..54873765hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38107552
hg19107552
hg18107552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042462
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)nssv3523864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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