A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367921



Internal ID21025474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17935325..17935917hg38UCSC Ensembl
chr3:17976817..17977409hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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