A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744161



Internal ID18718407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121649222..121649515hg38UCSC Ensembl
Outerchr9:121649160..121649584hg38UCSC Ensembl
Innerchr9:124411501..124411794hg19UCSC Ensembl
Outerchr9:124411439..124411863hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545414
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744161
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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