A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101787



Internal ID21285415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30284933..30286211hg38UCSC Ensembl
InnerchrX:30303050..30304328hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg381279
hg191279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111219
Supporting Variants
Samplessample373
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101787
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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