A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903661



Internal ID3257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32808117..32811796hg38UCSC Ensembl
chr1:33273718..33277397hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383680
hg193680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422250
Supporting Variants
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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