A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17214101



Internal ID21661610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60682422..60682422hg38UCSC Ensembl
chr11:60449895..60449895hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg388543
hg198543
Variant TypeCNV herv insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5702501
Supporting Variants
Samples
Known GenesLINC00301
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a HERV mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17214101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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