A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv27n21



Internal ID22766219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230610148..230613900hg38UCSC Ensembl
chr1:230745894..230749646hg19UCSC Ensembl
chr1:228812517..228816269hg18UCSC Ensembl
chr1:227052629..227056381hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg383753
hg193753
hg183753
hg173753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527218, nsv522630
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv27n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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