A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362284



Internal ID21019837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116726660..116727218hg38UCSC Ensembl
chr3:116445507..116446065hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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