A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17239773



Internal ID21687282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99654225..99654225hg38UCSC Ensembl
chr1:100119781..100119781hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716841
Supporting Variants
Samples
Known GenesPALMD
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)nssv17239773
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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