A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv106n21



Internal ID22766298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24993878..25005198hg38UCSC Ensembl
chr13:25568016..25579336hg19UCSC Ensembl
chr13:24466016..24477336hg18UCSC Ensembl
chr13:24466016..24477336hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3811321
hg1911321
hg1811321
hg1711321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521289, nsv515904
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv106n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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