A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353003



Internal ID22312884
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526588
Supporting Variants
SamplesNA19240
Known GenesPCDH11X
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353003
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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