A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677803



Internal ID21704124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36071262..36071262hg38UCSC Ensembl
chr1:36536863..36536863hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17203135, nssv17206477
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)nsv5677803
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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