A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749385



Internal ID18723631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68671171..68694365hg38UCSC Ensembl
Outerchr13:68666869..68695368hg38UCSC Ensembl
Innerchr13:69245303..69268497hg19UCSC Ensembl
Outerchr13:69241001..69269500hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3828500
hg1928500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749385
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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