A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv31n21



Internal ID22766223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235887907..235890872hg38UCSC Ensembl
chr1:236051207..236054172hg19UCSC Ensembl
chr1:234117830..234120795hg18UCSC Ensembl
chr1:232377248..232380213hg17UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382966
hg192966
hg182966
hg172966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524989, nsv517883
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv31n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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