A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363745



Internal ID21021298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167378559..167379219hg38UCSC Ensembl
chr3:167096347..167097007hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098114
Samples
Known GenesZBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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