A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908701



Internal ID6593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102611835..102642000hg38UCSC Ensembl
chr1:103077391..103107556hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3830166
hg1930166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908701
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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