A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227888



Internal ID20794928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29813901..29986400hg38UCSC Ensembl
chr6:29781678..29954177hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38172500
hg19172500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405513
Supporting Variants
Samples
Known GenesHCG4B, HCG9, HLA-A, HLA-G, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227888
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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