A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743316



Internal ID18717562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13572111..13575517hg38UCSC Ensembl
Outerchr9:13571295..13576058hg38UCSC Ensembl
Innerchr9:13572110..13575516hg19UCSC Ensembl
Outerchr9:13571294..13576057hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384764
hg194764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3544569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743316
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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