A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097687



Internal ID22006920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65487763..65487763hg38UCSC Ensembl
chr9:44764648..44764648hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097687
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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