A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226986



Internal ID20794026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29818301..29984000hg38UCSC Ensembl
chr6:29786078..29951777hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38165700
hg19165700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402572
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)nssv18226986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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