A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038830



Internal ID93635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122791194..122797323hg38UCSC Ensembl
chr10:124550710..124556839hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386130
hg196130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509048
Supporting Variants
Samples
Known GenesFLJ46361
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038830
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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