A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3522832



Internal ID22392256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67242127..67242462hg38UCSC Ensembl
chr15:67534465..67534800hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n152
Supporting Variantsnssv14376298, nssv14389351, nssv14379907, nssv14388706, nssv14386384
SamplesHG00512, HG00731, HG00732, HG00733, HG00514
Known GenesAAGAB
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)nsv3522832
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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