A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016111



Internal ID21925454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60618564..60618731hg38UCSC Ensembl
chr9_gl000199_random:100006..100173hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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