A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696202



Internal ID21722523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11056595..11056595hg38UCSC Ensembl
chr17:10959912..10959912hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17229927, nssv17199527
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)nsv5696202
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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