A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633959



Internal ID21826006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43662475..43693612hg38UCSC Ensembl
chr19:44166627..44197764hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3831138
hg1931138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060049
Supporting Variants
Samples
Known GenesPLAUR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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