A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398677



Internal ID178072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89692086..89692137hg38UCSC Ensembl
chr10:91451843..91451894hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036444
Samples
Known GenesFLJ37201
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398677
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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