A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558729



Internal ID22427532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85254317..85254631hg38UCSC Ensembl
chrX:84509323..84509637hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10178n152
Supporting Variantsnssv14352485, nssv14352484, nssv14352483
SamplesNA19238, NA19240, HG00513
Known GenesZNF711
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)nsv3558729
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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