A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373391



Internal ID21030944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82773558..82844135hg38UCSC Ensembl
chr3:82822709..82893286hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3870578
hg1970578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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