A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032933



Internal ID89651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57749116..57781323hg38UCSC Ensembl
chr10:59508876..59541083hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3832208
hg1932208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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