A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv232n21



Internal ID20131953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:184301745..185428608hg38UCSC Ensembl
chr2:185166472..186293335hg19UCSC Ensembl
chr2:184874717..186001580hg18UCSC Ensembl
chr2:184991978..186118841hg17UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381126864
hg191126864
hg181126864
hg171126864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522737, nsv528385
Samples
Known GenesZNF804A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv232n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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