A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236647



Internal ID21684156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15835737..15835737hg38UCSC Ensembl
chr1:16162232..16162232hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717808
Supporting Variants
Samples
Known GenesFLJ37453
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)nssv17236647
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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