A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527954



Internal ID18826235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68661514..68694098hg38UCSC Ensembl
Innerchr13:69235646..69268230hg19UCSC Ensembl
Innerchr13:68133647..68166231hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3832585
hg1932585
hg1832585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047512
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)nssv3527954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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