A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050703



Internal ID19139922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:32664185..32776907hg38UCSC Ensembl
Innerchr13:33238322..33351045hg19UCSC Ensembl
Innerchr13:32136322..32249045hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38112723
hg19112724
hg18112724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626n100
Supporting Variantsnssv3523236
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)nsv1050703
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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