A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526603



Internal ID18824884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63204173..63263121hg38UCSC Ensembl
Innerchr13:63778306..63837254hg19UCSC Ensembl
Innerchr13:62676307..62735255hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3858949
hg1958949
hg1858949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040676
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)nssv3526603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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