A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005356



Internal ID21914699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81612991..81613076hg38UCSC Ensembl
chr9:84227906..84227991hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578410
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005356
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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