A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360402



Internal ID21017955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46219878..46224207hg38UCSC Ensembl
chr3:46261369..46265698hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384330
hg194330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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