A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907927



Internal ID6068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8266438..8268570hg38UCSC Ensembl
chr1:8326498..8328630hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907927
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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