A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986576



Internal ID12634991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6471402..6918342hg38UCSC Ensembl
InnerchrX:6389443..6836383hg19UCSC Ensembl
InnerchrX:6399443..6846383hg18UCSC Ensembl
InnerchrX:6249179..6696119hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38446941
hg19446941
hg18446941
hg17446941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34585
Supporting Variants
SamplesNA18992
Known GenesVCX3A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986576
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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