A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586416



Internal ID7057798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147279247..147287120hg38UCSC Ensembl
InnerchrX:146360765..146368638hg19UCSC Ensembl
InnerchrX:146168457..146176330hg18UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg387874
hg197874
hg187874
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999927
Supporting Variants
SamplesHuRef
Known GenesMIR514A1, MIR514A2, MIR514A3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586416
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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