A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082143



Internal ID21991376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42601095..42601095hg38UCSC Ensembl
chr15:42893293..42893293hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614727
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082143
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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