A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908661



Internal ID6563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102190302..102393130hg38UCSC Ensembl
chr1:102655858..102858686hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38202829
hg19202829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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