A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032096



Internal ID89100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15497275..15501587hg38UCSC Ensembl
chr10:15539274..15543586hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384313
hg194313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476747
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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