A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506459



Internal ID20879739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41670198..41681596hg38UCSC Ensembl
chr17:39826450..39837848hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3811399
hg1911399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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