A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368676



Internal ID21026229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34908004..35229691hg38UCSC Ensembl
chr3:34949496..35271183hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38321688
hg19321688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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