A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550600



Internal ID18751676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64869579..64869969hg38UCSC Ensembl
Outerchr13:64869549..64870013hg38UCSC Ensembl
Innerchr13:65443711..65444101hg19UCSC Ensembl
Outerchr13:65443681..65444145hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749347
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550600
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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