A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632462



Internal ID21824509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18319442..18320544hg38UCSC Ensembl
chr19:18430252..18431354hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052785
Supporting Variants
Samples
Known GenesLSM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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