A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001727



Internal ID7066851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115843344..115889351hg38UCSC Ensembl
InnerchrX:114959677..115005684hg19UCSC Ensembl
InnerchrX:114865933..114919712hg18UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3846008
hg1946008
hg1853780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586638
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001727
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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