A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101682



Internal ID21280436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24497974..24500486hg38UCSC Ensembl
InnerchrX:24516091..24518603hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg382513
hg192513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115423
Supporting Variants
Samplessample299
Known GenesPDK3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101682
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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