A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007784



Internal ID6719895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42628258..42630969hg38UCSC Ensembl
Innerchr5:42628360..42631071hg19UCSC Ensembl
Innerchr5:42664117..42666828hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382712
hg192712
hg182712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv143e180
Supporting Variantsessv3586494
SamplesHuRef
Known GenesGHR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007784
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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