A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013216



Internal ID21922559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96300300..96300638hg38UCSC Ensembl
chr9:99062582..99062920hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590563
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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