A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926262



Internal ID22701489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34690970..35012521hg38UCSC Ensembl
chr10:34979898..35301449hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38321552
hg19321552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358488
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926262
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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