A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625405



Internal ID21817452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37968085..37968085hg38UCSC Ensembl
chr19:38458725..38458725hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103422
Supporting Variants
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625405
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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