A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17240490



Internal ID21687999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32423698..32423698hg38UCSC Ensembl
chr17:30750717..30750717hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5722136
Supporting Variants
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)nssv17240490
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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