A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720255



Internal ID21746576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39684350..39684350hg38UCSC Ensembl
chr15:39976551..39976551hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252021
Samples
Known GenesFSIP1
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)nsv5720255
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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