A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407168



Internal ID21064721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29765389..29993550hg38UCSC Ensembl
chr6:29733166..29961327hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38228162
hg19228162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6107n223
Supporting Variantsnssv18234613
Samples
Known GenesHCG4, HCG4B, HCG9, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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