A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014920



Internal ID21924263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79675268..79675397hg38UCSC Ensembl
chr9:82290183..82290312hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592379
Samples
Known GenesTLE4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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