A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550771



Internal ID18751847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82315126..82315398hg38UCSC Ensembl
Outerchr13:82315056..82315453hg38UCSC Ensembl
Innerchr13:82889261..82889533hg19UCSC Ensembl
Outerchr13:82889191..82889588hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749518
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550771
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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