A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv52n21



Internal ID18990525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128091905..128109225hg38UCSC Ensembl
chr10:129890169..129907489hg19UCSC Ensembl
chr10:129780159..129797479hg18UCSC Ensembl
chr10:129780159..129797479hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817321
hg1917321
hg1817321
hg1717321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516114, nsv523184
Samples
Known GenesMKI67
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv52n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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