A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038414



Internal ID93338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88132299..88132393hg38UCSC Ensembl
chr10:89892056..89892150hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.1138


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