A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041164



Internal ID95146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115974696..115980123hg38UCSC Ensembl
chr10:117734207..117739634hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385428
hg195428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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