A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009081



Internal ID21918424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33279670..33279797hg38UCSC Ensembl
chr9:33279668..33279795hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582435
Samples
Known GenesCHMP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009081
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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