A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359650



Internal ID21017203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4114287..4266910hg38UCSC Ensembl
chr3:4155971..4308594hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38152624
hg19152624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4773n223
Supporting Variantsnssv18099203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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