A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199770



Internal ID22349311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:356825..356920hg38UCSC Ensembl
chrX:317560..317655hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350453, nssv14350452, nssv14350454
SamplesNA19238, NA19239, NA19240
Known GenesPPP2R3B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199770
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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