A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206009



Internal ID22354619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107611303..107611712hg38UCSC Ensembl
chrX:106854533..106854942hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353855, nssv14353858, nssv14353856, nssv14353854, nssv14353857
SamplesNA19239, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206009
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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