A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17208723



Internal ID21656232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214771943..214771943hg38UCSC Ensembl
chr2:215636667..215636667hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5679944
Supporting Variants
Samples
Known GenesBARD1
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)nssv17208723
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer