A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367753



Internal ID21025306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36770168..36770886hg38UCSC Ensembl
chr3:36811659..36812377hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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