A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv230n21



Internal ID22766422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149086005..149092197hg38UCSC Ensembl
chr2:149942519..149948711hg19UCSC Ensembl
chr2:149650765..149656957hg18UCSC Ensembl
chr2:149768027..149774219hg17UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg386193
hg196193
hg186193
hg176193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521064, nsv527796
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv230n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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