A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626107



Internal ID21818154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19599280..19599280hg38UCSC Ensembl
chr19:19710089..19710089hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106588
Supporting Variants
Samples
Known GenesPBX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626107
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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