A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086439



Internal ID21995672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67043926..67043926hg38UCSC Ensembl
chr10:68803684..68803684hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381491
hg191491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588065
Samples
Known GenesCTNNA3, LRRTM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086439
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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