A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141402



Internal ID20708442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29892144..29946820hg38UCSC Ensembl
chr6:29859921..29914597hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854677
hg1954677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401821
Supporting Variants
Samples
Known GenesHCG4B, HLA-A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.12872


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