A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696000



Internal ID21722321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87782886..87782886hg38UCSC Ensembl
chr12:88176663..88176663hg19UCSC Ensembl
Cytoband12q21.32
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 Variantsnssv17193021
Samples
Known GenesMKRN9P
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)nsv5696000
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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