A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368550



Internal ID21026103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105722701..105724800hg38UCSC Ensembl
chr3:105441545..105443644hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093681
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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