A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749406



Internal ID18723652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69884985..69885244hg38UCSC Ensembl
Outerchr13:69884922..69885287hg38UCSC Ensembl
Innerchr13:70459117..70459376hg19UCSC Ensembl
Outerchr13:70459054..70459419hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550659
Supporting Variants
Samples
Known GenesKLHL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749406
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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