A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523871



Internal ID18822152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55741910..55981269hg38UCSC Ensembl
Innerchr13:56316044..56555403hg19UCSC Ensembl
Innerchr13:55214045..55453404hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38239360
hg19239360
hg18239360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047913
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)nssv3523871
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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