A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv143n21



Internal ID22766335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25873913..25881990hg38UCSC Ensembl
chr15:26119060..26127137hg19UCSC Ensembl
chr15:23670153..23678230hg18UCSC Ensembl
chr15:23670153..23678230hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg388078
hg198078
hg188078
hg178078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519720, nsv518809
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv143n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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