A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098953



Internal ID22008186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109519865..109519865hg38UCSC Ensembl
chr9:112282145..112282145hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098953
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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