A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037381



Internal ID19126600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:32664185..32783365hg38UCSC Ensembl
Innerchr13:33238322..33357503hg19UCSC Ensembl
Innerchr13:32136322..32255503hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38119181
hg19119182
hg18119182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626n100
Supporting Variantsnssv3523237
Samples
Known GenesPDS5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037381
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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