A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354909



Internal ID22282820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153830416..153832446hg38UCSC Ensembl
chrX:153095871..153097901hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382031
hg192031
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197821
Supporting Variants
SamplesNA19239
Known GenesPDZD4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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