A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749820



Internal ID18724066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109821203..109829153hg38UCSC Ensembl
Outerchr13:109820654..109829492hg38UCSC Ensembl
Innerchr13:110473550..110481500hg19UCSC Ensembl
Outerchr13:110473001..110481839hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg388839
hg198839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749820
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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