A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363965



Internal ID21021518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4098635..4164515hg38UCSC Ensembl
chr3:4140319..4206199hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3865881
hg1965881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4771n223
Supporting Variantsnssv18099189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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