A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038392



Internal ID93324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87824112..87824198hg38UCSC Ensembl
chr10:89583869..89583955hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143742
Supporting Variants
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038392
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012417


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