A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550694



Internal ID18751770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73500783..73501044hg38UCSC Ensembl
Outerchr13:73500756..73501111hg38UCSC Ensembl
Innerchr13:74074920..74075181hg19UCSC Ensembl
Outerchr13:74074893..74075248hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749441
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550694
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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