A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3523659



Internal ID22393087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35296796..35296943hg38UCSC Ensembl
chr15:35588997..35589144hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2894n152
Supporting Variantsnssv14386962, nssv14384106
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsAbsence of a ALUYB8 mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3523659
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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