A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14322126



Internal ID22266362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93341435..93341747hg38UCSC Ensembl
chr5:92677141..92677453hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV alu deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177997
Supporting Variants
SamplesNA19238
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)nssv14322126
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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