A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099238



Internal ID22008471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11682664..11682664hg38UCSC Ensembl
chr10:11724663..11724663hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099238
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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