A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367959



Internal ID21025512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17933199..17933687hg38UCSC Ensembl
chr3:17974691..17975179hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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