A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369207



Internal ID21026760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81976154..81976632hg38UCSC Ensembl
chr3:82025305..82025783hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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