A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032365



Internal ID89275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8868839..8868955hg38UCSC Ensembl
chr10:8910802..8910918hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032365
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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