A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367818



Internal ID21025371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74880626..74885584hg38UCSC Ensembl
chr3:74929777..74934735hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg384959
hg194959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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