A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033594



Internal ID90086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19493642..19696691hg38UCSC Ensembl
chr10:19782571..19985620hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38203050
hg19203050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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