A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018092



Internal ID21927435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129519025..129520578hg38UCSC Ensembl
chr9:132281304..132282857hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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