A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085649



Internal ID21994882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66309094..66309094hg38UCSC Ensembl
chr15:66601432..66601432hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598103
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085649
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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