A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1617n100



Internal ID20153233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24445874..24467049hg38UCSC Ensembl
chr13:25020012..25041187hg19UCSC Ensembl
chr13:23918012..23939187hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3821176
hg1921176
hg1821176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036700, nsv1038671, nsv1044637, nsv1049555, nsv1050785
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)dgv1617n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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