A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565034



Internal ID7036134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:80608039..80619342hg38UCSC Ensembl
Outerchr9:83222954..83234257hg19UCSC Ensembl
Outerchr9:82412774..82424077hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3811304
hg1911304
hg1811304
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992199
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565034
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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