A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398733



Internal ID21056286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29793191..29949321hg38UCSC Ensembl
chr6:29760968..29917098hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156131
hg19156131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6110n223
Supporting Variantsnssv18218500
Samples
Known GenesHCG4B, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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