A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367111



Internal ID21024664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165213001..165213800hg38UCSC Ensembl
chr3:164930789..164931588hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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