A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031716



Internal ID88865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20546225..20715429hg38UCSC Ensembl
chr10:20835154..21004358hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38169205
hg19169205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475498
Supporting Variants
Samples
Known GenesMIR4675
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031716
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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