A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564796



Internal ID18765872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151419650..151420326hg38UCSC Ensembl
Outerchr4:151419483..151420475hg38UCSC Ensembl
Innerchr4:152340802..152341478hg19UCSC Ensembl
Outerchr4:152340635..152341627hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763543
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564796
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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