A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743552



Internal ID18371112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35662946..35664362hg38UCSC Ensembl
Outerchr9:35662936..35664587hg38UCSC Ensembl
Innerchr9:35662943..35664359hg19UCSC Ensembl
Outerchr9:35662933..35664584hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3544805
Supporting Variants
Samples
Known GenesARHGEF39
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743552
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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