A curated catalogue of human genomic structural variation




Variant Details

Variant: esv33517



Internal ID1682866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:18679168..19146187hg19UCSC Ensembl
InnerchrX:18589089..19056108hg18UCSC Ensembl
InnerchrX:18438825..18905844hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv99383, essv99804, essv96672, essv99204
Samples22335, 22086, 22011, 22275
Known GenesGPR64, LOC100132163, PHKA2, PPEF1, RS1
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv33517
Frequency
Sample Size51
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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