A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038797



Internal ID93609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121712148..121717090hg38UCSC Ensembl
chr10:123471662..123476604hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384943
hg194943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038797
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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