A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709800



Internal ID21736121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64492781..64492781hg38UCSC Ensembl
chr16:64526684..64526684hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17199359
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5709800
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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