A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005618



Internal ID7070713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179632876..179662422hg38UCSC Ensembl
Outerchr5:179059877..179089423hg19UCSC Ensembl
Outerchr5:178992483..179022029hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3829547
hg1929547
hg1829547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565755
SamplesHuRef
Known GenesC5orf60
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005618
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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