A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734802



Internal ID158468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37968592..37969748hg38UCSC Ensembl
chr21:39340895..39342051hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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