A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141772



Internal ID340969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40002000..40159000hg38UCSC Ensembl
chr9:42147018..42304018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38157001
hg19157001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141772
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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