A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036700



Internal ID18779231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24449798..24467049hg38UCSC Ensembl
Innerchr13:25023936..25041187hg19UCSC Ensembl
Innerchr13:23921936..23939187hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3817252
hg1917252
hg1817252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1617n100
Supporting Variantsnssv3523183
Samples
Known GenesPARP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036700
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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