A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744279



Internal ID18718525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130876782..130877661hg38UCSC Ensembl
Outerchr9:130876726..130877865hg38UCSC Ensembl
Innerchr9:133752169..133753048hg19UCSC Ensembl
Outerchr9:133752113..133753252hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545532
Supporting Variants
Samples
Known GenesABL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744279
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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