A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042217



Internal ID95856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131278556..131281791hg38UCSC Ensembl
chr10:133076819..133080054hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559442
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042217
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.026382


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