A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv36n21



Internal ID22766228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5711774..5726530hg38UCSC Ensembl
chr10:5753737..5768493hg19UCSC Ensembl
chr10:5793743..5808499hg18UCSC Ensembl
chr10:5793743..5808499hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814757
hg1914757
hg1814757
hg1714757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519891, nsv525080
Samples
Known GenesFAM208B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv36n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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