A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011383



Internal ID7060145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69927838..69941093hg38UCSC Ensembl
Outerchr9:72542754..72556009hg19UCSC Ensembl
Outerchr9:71732574..71745829hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3813256
hg1913256
hg1813256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563647
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011383
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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