A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3995n223



Internal ID22806963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89839977..90402500hg38UCSC Ensembl
chr2:89878787..90321525hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38562524
hg19442739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6346696, nsv6353627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3995n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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