A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526037



Internal ID22395416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22017588..22022652hg38UCSC Ensembl
chrX:22035706..22040770hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385065
hg195065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350022, nssv14350021
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526037
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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