A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084059



Internal ID21993292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:657214..657214hg38UCSC Ensembl
chr10:703154..703154hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579660
Samples
Known GenesDIP2C, PRR26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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