A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036409



Internal ID92021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89253315..89255301hg38UCSC Ensembl
chr10:91013072..91015058hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381987
hg191987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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