A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5724865



Internal ID21751186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124237649..124237649hg38UCSC Ensembl
chr10:125926218..125926218hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17252798, nssv17241489
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)nsv5724865
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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