A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097650



Internal ID20664690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185011951..185033012hg38UCSC Ensembl
chr3:184729739..184750800hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3821062
hg1921062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368384
Supporting Variants
Samples
Known GenesVPS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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