A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141400



Internal ID20708440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29888695..29943445hg38UCSC Ensembl
chr6:29856472..29911222hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854751
hg1954751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404865
Supporting Variants
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.12872


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer