A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011141



Internal ID21920484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83272680..83272796hg38UCSC Ensembl
chr9:85887595..85887711hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590488
Samples
Known GenesFRMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011141
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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