A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366387



Internal ID21023940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18127688..18128896hg38UCSC Ensembl
chr3:18169180..18170388hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097775
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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