A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2649n223



Internal ID22805617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99870660..100381017hg38UCSC Ensembl
chr15:100410865..100921222hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38510358
hg19510358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6495758, nsv6498742
Samples
Known GenesADAMTS17, SPATA41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2649n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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