A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988749



Internal ID7060580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26497343..26504152hg38UCSC Ensembl
InnerchrX:26515460..26522269hg19UCSC Ensembl
InnerchrX:26425381..26432190hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg386810
hg196810
hg186810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586335
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988749
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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