A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552075



Internal ID18406465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102172174..102172864hg38UCSC Ensembl
Outerchr14:102172051..102172875hg38UCSC Ensembl
Innerchr14:102638511..102639201hg19UCSC Ensembl
Outerchr14:102638388..102639212hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750822
Samples
Known GenesWDR20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552075
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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