A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236980



Internal ID21684489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157210428..157210428hg38UCSC Ensembl
chr1:157180218..157180218hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5725274
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)nssv17236980
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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