A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17234443



Internal ID21681952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27428495..27428495hg38UCSC Ensembl
chr7:27468114..27468114hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5723208
Supporting Variants
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17234443
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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