A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997659



Internal ID6733600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30377847..30425897hg38UCSC Ensembl
Innerchr15:30670050..30718100hg19UCSC Ensembl
Innerchr15:28457342..28505392hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3848051
hg1948051
hg1848051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586418
SamplesHuRef
Known GenesCHRFAM7A, LOC101059918
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997659
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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