A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749991



Internal ID18724237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23705845..23706131hg38UCSC Ensembl
Outerchr14:23705787..23706169hg38UCSC Ensembl
Innerchr14:24175054..24175340hg19UCSC Ensembl
Outerchr14:24174996..24175378hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749991
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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