A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009924



Internal ID6722016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25258945..25338322hg38UCSC Ensembl
Innerchr1:25585436..25664813hg19UCSC Ensembl
Innerchr1:25458023..25537400hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3879378
hg1979378
hg1879378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3e180
Supporting Variantsessv3586142
SamplesHuRef
Known GenesRHD, TMEM50A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009924
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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