A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052564



Internal ID102895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114587124..114632798hg38UCSC Ensembl
chr11:114457846..114503520hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3845675
hg1945675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493969
Supporting Variants
Samples
Known GenesNXPE4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052564
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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