A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565388



Internal ID7036770
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008507
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565388
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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