A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039672



Internal ID94167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111793000..111798368hg38UCSC Ensembl
chr10:113552758..113558126hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385369
hg195369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000469


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