A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356693



Internal ID21014246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80061001..80062400hg38UCSC Ensembl
chr3:80110151..80111550hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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