A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739905



Internal ID5050637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3609420..3609547hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6849882, essv6957815
SamplesSSM086, SSM026
Known GenesPRKX
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2739905
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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