A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239597



Internal ID21687106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109129836..109129836hg38UCSC Ensembl
chr6:109451039..109451039hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722814
Supporting Variants
Samples
Known GenesCEP57L1
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)nssv17239597
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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