A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906539



Internal ID5150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96609464..96656561hg38UCSC Ensembl
chr1:97075020..97122117hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3847098
hg1947098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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