A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090881



Internal ID22000114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71057484..71057484hg38UCSC Ensembl
chr15:71349823..71349823hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090881
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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