A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007887



Internal ID6719997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155560007..155573754hg38UCSC Ensembl
OuterchrX:154789668..154803415hg19UCSC Ensembl
OuterchrX:154442862..154456609hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813748
hg1913748
hg1813748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565653
SamplesHuRef
Known GenesTMLHE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007887
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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