A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv198n21



Internal ID22766390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8985576..8990996hg38UCSC Ensembl
chr19:9096252..9101672hg19UCSC Ensembl
chr19:8957252..8962672hg18UCSC Ensembl
chr19:8957252..8962672hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385421
hg195421
hg185421
hg175421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526942, nsv522984
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv198n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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