A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586492



Internal ID7057874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62506452..62700763hg38UCSC Ensembl
InnerchrX:61725922..61920233hg19UCSC Ensembl
InnerchrX:61642647..61836958hg18UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38194312
hg19194312
hg18194312
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005217
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586492
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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