A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367165



Internal ID21024718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58532455..58539986hg38UCSC Ensembl
chr3:58518182..58525713hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg387532
hg197532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102946
Samples
Known GenesACOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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