A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056617



Internal ID21965850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33056844..33057425hg38UCSC Ensembl
chr19:33547750..33548331hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636208
Samples
Known GenesRHPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056617
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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