A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750414



Internal ID18724660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65152360..65153500hg38UCSC Ensembl
Outerchr14:65152342..65153607hg38UCSC Ensembl
Innerchr14:65619078..65620218hg19UCSC Ensembl
Outerchr14:65619060..65620325hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750414
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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