A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101793



Internal ID21285954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24497974..24503144hg38UCSC Ensembl
InnerchrX:24516091..24521261hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385171
hg195171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112787
Supporting Variants
Samplessample380
Known GenesPDK3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101793
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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