A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036227



Internal ID91896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58903356..58907550hg38UCSC Ensembl
chr10:60663116..60667310hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384195
hg194195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036227
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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