A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096707



Internal ID22005940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36322320..36322320hg38UCSC Ensembl
chr15:36614521..36614521hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096707
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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