A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978258



Internal ID12634988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6577241..6903064hg38UCSC Ensembl
InnerchrX:6495282..6821105hg19UCSC Ensembl
InnerchrX:6505282..6831105hg18UCSC Ensembl
InnerchrX:6355018..6680841hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38325824
hg19325824
hg18325824
hg17325824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34585
Supporting Variants
SamplesNA18992
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978258
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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