A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037215



Internal ID92559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83904285..83905897hg38UCSC Ensembl
chr10:85664041..85665653hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037215
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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