A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413158



Internal ID21070711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29895426..29952661hg38UCSC Ensembl
chr6:29863203..29920438hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3857236
hg1957236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6117n223
Supporting Variantsnssv18141404
Samples
Known GenesHCG4B, HLA-A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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