A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368864



Internal ID21026417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59108138..59152253hg38UCSC Ensembl
chr3:59093864..59137979hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3844116
hg1944116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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