A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561819



Internal ID18762895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45726893..45727122hg38UCSC Ensembl
Outerchr3:45726852..45727199hg38UCSC Ensembl
Innerchr3:45768385..45768614hg19UCSC Ensembl
Outerchr3:45768344..45768691hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760566
Samples
Known GenesSACM1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561819
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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