A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5721548



Internal ID21747869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158086601..158086601hg38UCSC Ensembl
chr6:158507633..158507633hg19UCSC Ensembl
Cytoband6q25.3
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 Variantsnssv17252993
Samples
Known GenesSYNJ2
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)nsv5721548
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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