A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231491



Internal ID20798531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29794315..29950529hg38UCSC Ensembl
chr6:29762092..29918306hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156215
hg19156215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415275
Supporting Variants
Samples
Known GenesHCG4B, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00012


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