A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5727059



Internal ID21753380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15666351..15666351hg38UCSC Ensembl
chr1:15992846..15992846hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17249037
Samples
Known Genes
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)nsv5727059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer