A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037959



Internal ID93055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94179156..94184416hg38UCSC Ensembl
chr10:95938913..95944173hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385261
hg195261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487629
Supporting Variants
Samples
Known GenesPLCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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