A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3549236



Internal ID18750312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:53851636..53851900hg38UCSC Ensembl
Outerchr12:53851584..53851965hg38UCSC Ensembl
Innerchr12:54245420..54245684hg19UCSC Ensembl
Outerchr12:54245368..54245749hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747983
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3549236
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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