A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365125



Internal ID21022678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38224401..38227100hg38UCSC Ensembl
chr3:38265892..38268591hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100815
Samples
Known GenesOXSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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