A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620302



Internal ID21812349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38132731..38132791hg38UCSC Ensembl
chr19:38623371..38623431hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040765
Supporting Variants
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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