A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082323



Internal ID21991556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126120932..126120932hg38UCSC Ensembl
chr10:127809501..127809501hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592115
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082323
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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