A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982434



Internal ID55643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27132731..27133715hg38UCSC Ensembl
chr6:27100510..27101494hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473084
Supporting Variants
Samples
Known GenesHIST1H2AG, HIST1H2BJ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982434
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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