A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5718694



Internal ID21745015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17354434..17354434hg38UCSC Ensembl
chr19:17465243..17465243hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17233455, nssv17235882
Samples
Known GenesPLVAP
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)nsv5718694
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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