A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998832



Internal ID7064585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81803926..81812519hg38UCSC Ensembl
Outerchr9:84418841..84427434hg19UCSC Ensembl
Outerchr9:83608661..83617254hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg388594
hg198594
hg188594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564213
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998832
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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