A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17189628



Internal ID21637137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86864757..86864757hg38UCSC Ensembl
chr10:88624514..88624514hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5700775
Supporting Variants
Samples
Known GenesBMPR1A
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)nssv17189628
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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