A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353719



Internal ID22579388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62087298..62087298hg38UCSC Ensembl
chr10:63847057..63847057hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954514
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353719
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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