A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091680



Internal ID22000913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88187147..88187147hg38UCSC Ensembl
chr10:89946904..89946904hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091680
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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