A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096342



Internal ID22005575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67812103..67812103hg38UCSC Ensembl
chr10:69571861..69571861hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382173
hg192173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577556
Samples
Known GenesDNAJC12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096342
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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