A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958493



Internal ID22733555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69332384..69332384hg38UCSC Ensembl
chr10:71092140..71092140hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351004
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958493
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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