A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361085



Internal ID21018638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43817572..43822843hg38UCSC Ensembl
chr3:43859064..43864335hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg385272
hg195272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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