A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095718



Internal ID22004951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79798170..79798170hg38UCSC Ensembl
chr9:82413085..82413085hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095718
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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