A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523385



Internal ID18821666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39160951..39265120hg38UCSC Ensembl
Innerchr13:39735088..39839257hg19UCSC Ensembl
Innerchr13:38633088..38737257hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38104170
hg19104170
hg18104170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047276
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)nssv3523385
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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