A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007127



Internal ID7072220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103682974..103684468hg38UCSC Ensembl
Innerchr10:105442732..105444226hg19UCSC Ensembl
Innerchr10:105432722..105434216hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381495
hg191495
hg181495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586964
SamplesHuRef
Known GenesSH3PXD2A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007127
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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