A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058320



Internal ID21967555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45106244..45119156hg38UCSC Ensembl
chr19:45609502..45622414hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3812913
hg1912913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623047
Samples
Known GenesPPP1R37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058320
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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