A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983580



Internal ID12976522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5140939..5669353hg38UCSC Ensembl
InnerchrX:5058980..5587394hg19UCSC Ensembl
InnerchrX:5068980..5597394hg18UCSC Ensembl
InnerchrX:4918716..5447130hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38528415
hg19528415
hg18528415
hg17528415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752328
Supporting Variants
SamplesBEC_669
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983580
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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