A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901199



Internal ID1610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27662819..27662872hg38UCSC Ensembl
chr1:27989330..27989383hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901199
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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