A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500574



Internal ID20873801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41191774..41193988hg38UCSC Ensembl
chr17:39348026..39350240hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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