A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526367



Internal ID22395748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233763..47233816hg38UCSC Ensembl
chrX:47093162..47093215hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351128, nssv14351127, nssv14351129, nssv14351130
SamplesHG00732, HG00733, HG00513, HG00514
Known GenesUSP11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526367
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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