A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097093



Internal ID22006326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112195126..112195126hg38UCSC Ensembl
chr10:113954884..113954884hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383025
hg193025
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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