A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369091



Internal ID21026644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6401019..6409222hg38UCSC Ensembl
chr3:6442706..6450909hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg388204
hg198204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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