A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744233



Internal ID18718479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128356719..128356846hg38UCSC Ensembl
Outerchr9:128356700..128356850hg38UCSC Ensembl
Innerchr9:131118998..131119125hg19UCSC Ensembl
Outerchr9:131118979..131119129hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545486
Supporting Variants
Samples
Known GenesSLC27A4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744233
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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