A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368384



Internal ID21025937
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 StatusM
Merged Variants
Supporting Variantsnssv18097650
Samples
Known GenesVPS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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