A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412899



Internal ID21070452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22200682..22258777hg38UCSC Ensembl
chr6:22200911..22259006hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3858096
hg1958096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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