A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696827



Internal ID21723148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64135278..64135278hg38UCSC Ensembl
chr16:64169182..64169182hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17199351
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)nsv5696827
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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