A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624657



Internal ID21816704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33458052..33458847hg38UCSC Ensembl
chr19:33948958..33949753hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056750
Supporting Variants
Samples
Known GenesPEPD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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