A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052482



Internal ID19141701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66088384..66122527hg38UCSC Ensembl
Innerchr13:66662516..66696659hg19UCSC Ensembl
Innerchr13:65560517..65594660hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3834144
hg1934144
hg1834144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527919
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)nsv1052482
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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