A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365314



Internal ID21022867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181156844..181160913hg38UCSC Ensembl
chr3:180874632..180878701hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384070
hg194070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097763
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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