A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084097



Internal ID21993330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19819354..19819354hg38UCSC Ensembl
chr10:20108283..20108283hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596368
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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