A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564194



Internal ID18418584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86842815..86842870hg38UCSC Ensembl
Outerchr4:86842813..86842874hg38UCSC Ensembl
Innerchr4:87763968..87764023hg19UCSC Ensembl
Outerchr4:87763966..87764027hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762941
Samples
Known GenesSLC10A6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564194
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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