A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890097



Internal ID167542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9155277..9155728hg38UCSC Ensembl
chr1:9215336..9215787hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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