A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2369n223



Internal ID22805337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17050201..17075500hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3825300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6496985, nsv6497358, nsv6500202, nsv6498307, nsv6514569, nsv6506673, nsv6509567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2369n223
Frequency
Sample Size19652
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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