A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2628n223



Internal ID22805596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92713829..92777033hg38UCSC Ensembl
chr15:93257059..93320263hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3863205
hg1963205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6506680, nsv6511426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2628n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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