A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000883



Internal ID6713025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180616250..180618421hg38UCSC Ensembl
Innerchr5:180043250..180045421hg19UCSC Ensembl
Innerchr5:179975856..179978027hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382172
hg192172
hg182172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586532
SamplesHuRef
Known GenesFLT4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000883
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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