A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082366



Internal ID21991599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57687410..57687410hg38UCSC Ensembl
chr10:59447170..59447170hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082366
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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