A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351128



Internal ID22157068
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526367
Supporting Variants
SamplesHG00514
Known GenesUSP11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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