A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3911n223



Internal ID22806879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66243101..66250200hg38UCSC Ensembl
chr2:66470233..66477332hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6338725, nsv6344545, nsv6342814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3911n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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