A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273248



Internal ID20482466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17150570..17151005hg38UCSC Ensembl
chr19:17261380..17261815hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745498
Supporting Variants
Samples
Known GenesMYO9B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273248
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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