A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374847



Internal ID21032400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3234766..3287434hg38UCSC Ensembl
chr3:3276450..3329118hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3852669
hg1952669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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