A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033458



Internal ID89993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28985119..28987493hg38UCSC Ensembl
chr10:29274048..29276422hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033458
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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