A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141384



Internal ID20708424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29804733..29959858hg38UCSC Ensembl
chr6:29772510..29927635hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38155126
hg19155126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396925
Supporting Variants
Samples
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00893


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