A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039696



Internal ID94186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112193964..112194031hg38UCSC Ensembl
chr10:113953722..113953789hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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