A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619600



Internal ID21811647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38808461..38808547hg38UCSC Ensembl
chr19:39299101..39299187hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054206
Supporting Variants
Samples
Known GenesLGALS4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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