A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711832



Internal ID19010113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63850118..64363338hg38UCSC Ensembl
Innerchr13:64424251..64937470hg19UCSC Ensembl
Innerchr13:63322252..63835471hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38513221
hg19513220
hg18513220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037078
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)nssv3711832
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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