A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523399



Internal ID18821680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42630604..42651585hg38UCSC Ensembl
Innerchr13:43204740..43225721hg19UCSC Ensembl
Innerchr13:42102740..42123721hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3820982
hg1920982
hg1820982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041476
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)nssv3523399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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