A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626062



Internal ID21818109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41269399..41269585hg38UCSC Ensembl
chr19:41775304..41775490hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047334
Supporting Variants
Samples
Known GenesHNRNPUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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