A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008507



Internal ID7073484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:60945093..60959453hg38UCSC Ensembl
Outerchr8:61857652..61872012hg19UCSC Ensembl
Outerchr8:62020206..62034566hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3814361
hg1914361
hg1814361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565388
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008507
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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