A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013138



Internal ID21922481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29765460..29993533hg38UCSC Ensembl
chr6:29733237..29961310hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38228074
hg19228074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573103
Samples
Known GenesHCG4, HCG4B, HCG9, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013138
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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