A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545413



Internal ID18746489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121642908..121643796hg38UCSC Ensembl
Outerchr9:121642887..121643843hg38UCSC Ensembl
Innerchr9:124405187..124406075hg19UCSC Ensembl
Outerchr9:124405166..124406122hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744160
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545413
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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