A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5720206



Internal ID21746527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45454757..45454757hg38UCSC Ensembl
chr10:45950205..45950205hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17248912
Samples
Known GenesMARCH8
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)nsv5720206
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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