A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093102



Internal ID22002335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31765768..31765768hg38UCSC Ensembl
chr10:32054696..32054696hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093102
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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