A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv45n21



Internal ID22766237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69650087..69655485hg38UCSC Ensembl
chr10:71409843..71415241hg19UCSC Ensembl
chr10:71079849..71085247hg18UCSC Ensembl
chr10:71079849..71085247hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385399
hg195399
hg185399
hg175399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518224, nsv521284
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv45n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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