A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395658



Internal ID21053211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29800033..29956338hg38UCSC Ensembl
chr6:29767810..29924115hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156306
hg19156306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6110n223
Supporting Variantsnssv18222387
Samples
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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