A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907756



Internal ID5950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106326208..106420119hg38UCSC Ensembl
chr1:106868830..106962741hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3893912
hg1993912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907756
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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