A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750501



Internal ID18724747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72866248..72867091hg38UCSC Ensembl
Outerchr14:72866045..72867159hg38UCSC Ensembl
Innerchr14:73332956..73333799hg19UCSC Ensembl
Outerchr14:73332753..73333867hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551754
Supporting Variants
Samples
Known GenesDPF3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750501
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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