A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17235933



Internal ID21683442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34301334..34301334hg38UCSC Ensembl
chr19:34792239..34792239hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722361
Supporting Variants
Samples
Known GenesKIAA0355
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a SVA mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17235933
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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