A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090312



Internal ID21999545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24978803..24978803hg38UCSC Ensembl
chr10:25267732..25267732hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090312
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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