A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5721668



Internal ID21747989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135359453..135359453hg38UCSC Ensembl
chr5:134695143..134695143hg19UCSC Ensembl
Cytoband5q31.1
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 Variantsnssv17240823
Samples
Known GenesH2AFY
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)nsv5721668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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