A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141399



Internal ID20708439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29886014..29940824hg38UCSC Ensembl
chr6:29853791..29908601hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854811
hg1954811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408681
Supporting Variants
Samples
Known GenesHCG4B, HLA-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.13631


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