A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206773



Internal ID22355263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40046522..40046576hg38UCSC Ensembl
chrX:39905775..39905829hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10089n152
Supporting Variantsnssv14350288, nssv14350290, nssv14350289
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206773
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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