A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525593



Internal ID22394971
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354887, nssv14354886, nssv14354888
SamplesNA19238, NA19239, NA19240
Known GenesHAUS7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525593
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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