A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203513



Internal ID22352510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10032831..10032980hg38UCSC Ensembl
chrX:10000871..10001020hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349864
SamplesNA19239
Known GenesWWC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203513
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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