A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5719903



Internal ID21746224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68812048..68812048hg38UCSC Ensembl
chr15:69104387..69104387hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252972, nssv17235750
Samples
Known GenesANP32A
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)nsv5719903
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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