A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3891n223



Internal ID22806859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57956523..57988023hg38UCSC Ensembl
chr2:58183658..58215158hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3831501
hg1931501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6354424, nsv6350704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3891n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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