A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552013



Internal ID18406403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96393931..96394758hg38UCSC Ensembl
Outerchr14:96393891..96394788hg38UCSC Ensembl
Innerchr14:96860268..96861095hg19UCSC Ensembl
Outerchr14:96860228..96861125hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750760
Samples
Known GenesAK7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552013
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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