A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761919



Internal ID18736165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196031749..196032967hg38UCSC Ensembl
Outerchr3:196031743..196032972hg38UCSC Ensembl
Innerchr3:195758620..195759838hg19UCSC Ensembl
Outerchr3:195758614..195759843hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381230
hg191230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563172
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761919
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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