A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv229n21



Internal ID22766421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:140583057..140592531hg38UCSC Ensembl
chr2:141340626..141350100hg19UCSC Ensembl
chr2:141057096..141066570hg18UCSC Ensembl
chr2:141174358..141183832hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg389475
hg199475
hg189475
hg179475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520152, nsv528618
Samples
Known GenesLRP1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv229n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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