A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891010



Internal ID168182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157984655..157984767hg38UCSC Ensembl
chr1:157954445..157954557hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891010
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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