A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368882



Internal ID22594551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16978469..17011973hg38UCSC Ensembl
chr10:17020468..17053972hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3833505
hg1933505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912730
Supporting Variants
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368882
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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