A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081143



Internal ID21990376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:322921..322921hg38UCSC Ensembl
chr10:368861..368861hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591554
Samples
Known GenesDIP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081143
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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