A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv663n223



Internal ID22803631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26602401..26695016hg38UCSC Ensembl
chr10:26891330..26983945hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3892616
hg1992616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6436876, nsv6450410
Samples
Known GenesLINC00202-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv663n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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