A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086639



Internal ID21995872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71769016..71769016hg38UCSC Ensembl
chr15:72061355..72061355hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606167
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086639
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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