A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032089



Internal ID89094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15470960..15473364hg38UCSC Ensembl
chr10:15512959..15515363hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032089
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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