A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5722456



Internal ID21748777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102668086..102668086hg38UCSC Ensembl
chr14:103134423..103134423hg19UCSC Ensembl
Cytoband14q32.31
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 Variantsnssv17248056, nssv17235471
Samples
Known GenesRCOR1
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)nsv5722456
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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