A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038396



Internal ID93327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87840380..87842984hg38UCSC Ensembl
chr10:89600137..89602741hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382605
hg192605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484877
Supporting Variants
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038396
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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