A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989820



Internal ID12976526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5140943..5669353hg38UCSC Ensembl
InnerchrX:5058984..5587394hg19UCSC Ensembl
InnerchrX:5068984..5597394hg18UCSC Ensembl
InnerchrX:4918720..5447130hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38528411
hg19528411
hg18528411
hg17528411
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)essv6989820
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer