A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141689



Internal ID340886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65815191..65827000hg38UCSC Ensembl
chr9:42795768..42807578hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3811810
hg1911811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141689
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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