A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002297



Internal ID7067413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:82736535..82745330hg38UCSC Ensembl
Outerchr9:85351450..85360245hg19UCSC Ensembl
Outerchr9:84541270..84550065hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg388796
hg198796
hg188796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565082
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002297
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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