A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564728



Internal ID18765804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141005795..141006051hg38UCSC Ensembl
Outerchr4:141005743..141006115hg38UCSC Ensembl
Innerchr4:141926949..141927205hg19UCSC Ensembl
Outerchr4:141926897..141927269hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763475
Samples
Known GenesRNF150
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564728
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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