A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899999



Internal ID775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17444118..17452132hg38UCSC Ensembl
chr1:17770614..17778628hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg388015
hg198015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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