A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv117n21



Internal ID22766309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93048422..93060867hg38UCSC Ensembl
chr13:93700675..93713120hg19UCSC Ensembl
chr13:92498676..92511121hg18UCSC Ensembl
chr13:92498676..92511121hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3812446
hg1912446
hg1812446
hg1712446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526346, nsv519671
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv117n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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