A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526588



Internal ID22395969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92112536..92113796hg38UCSC Ensembl
chrX:91367535..91368795hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353002, nssv14353003
SamplesNA19238, NA19240
Known GenesPCDH11X
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526588
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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