A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559593



Internal ID332623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117739638..117739647hg38UCSC Ensembl
chr10:119499149..119499158hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3810
hg1910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559593
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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