A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036892



Internal ID92351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91363271..91366525hg38UCSC Ensembl
chr10:93123028..93126282hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383255
hg193255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486815
Supporting Variants
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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