A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367551



Internal ID21025104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122831965..122832636hg38UCSC Ensembl
chr3:122550812..122551483hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095215
Samples
Known GenesDIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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