A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989178



Internal ID7075992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114066645..114071276hg38UCSC Ensembl
Outerchr9:116828925..116833556hg19UCSC Ensembl
Outerchr9:115868746..115873377hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg384632
hg194632
hg184632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563685
SamplesHuRef
Known GenesAMBP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989178
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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