A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367376



Internal ID21024929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34342595..34343205hg38UCSC Ensembl
chr3:34384087..34384697hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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