A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv234n21



Internal ID22766426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194395007..194508560hg38UCSC Ensembl
chr2:195259731..195373284hg19UCSC Ensembl
chr2:194967976..195081529hg18UCSC Ensembl
chr2:195085237..195198790hg17UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38113554
hg19113554
hg18113554
hg17113554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521844, nsv526272
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv234n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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