A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053937



Internal ID21963171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17134031..17134658hg38UCSC Ensembl
chr19:17244841..17245468hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637525
Samples
Known GenesMYO9B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053937
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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