A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038132



Internal ID19127351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52483224..52616859hg38UCSC Ensembl
Innerchr13:53057359..53190994hg19UCSC Ensembl
Innerchr13:51955360..52088995hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38133636
hg19133636
hg18133636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523467, nssv3523468
Samples
Known GenesTPTE2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038132
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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