A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586078



Internal ID7057460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:37478196..37485073hg38UCSC Ensembl
InnerchrX:37337449..37344326hg19UCSC Ensembl
InnerchrX:37222370..37229247hg18UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386878
hg196878
hg186878
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007820
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586078
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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