A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv660n223



Internal ID22803628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26572560..26643467hg38UCSC Ensembl
chr10:26861489..26932396hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3870908
hg1970908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6435863, nsv6453106, nsv6443516, nsv6448305
Samples
Known GenesLINC00202-2, LINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv660n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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