A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373056



Internal ID21030609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82660503..82720889hg38UCSC Ensembl
chr3:82709654..82770040hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3860387
hg1960387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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