A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082068



Internal ID21991301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21430531..21430531hg38UCSC Ensembl
chr10:21719460..21719460hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082068
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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