A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564761



Internal ID18765837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146809104..146809796hg38UCSC Ensembl
Outerchr4:146808953..146809979hg38UCSC Ensembl
Innerchr4:147730256..147730948hg19UCSC Ensembl
Outerchr4:147730105..147731131hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763508
Samples
Known GenesTTC29
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564761
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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