A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032730



Internal ID89513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43066772..43073930hg38UCSC Ensembl
chr10:43562220..43569378hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387159
hg197159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032730
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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