A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354887



Internal ID22282800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153481271..153481323hg38UCSC Ensembl
chrX:152746729..152746781hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525593
Supporting Variants
SamplesNA19239
Known GenesHAUS7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354887
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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