A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097420



Internal ID22006653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8985436..8985436hg38UCSC Ensembl
chr10:9027399..9027399hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097420
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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