A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750507



Internal ID18724753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73061114..73064958hg38UCSC Ensembl
Outerchr14:73060141..73065334hg38UCSC Ensembl
Innerchr14:73527822..73531666hg19UCSC Ensembl
Outerchr14:73526849..73532042hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg385194
hg195194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551760
Supporting Variants
Samples
Known GenesRBM25
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750507
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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