A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9748881



Internal ID18376441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20710366..20711119hg38UCSC Ensembl
Outerchr13:20710348..20711136hg38UCSC Ensembl
Innerchr13:21284505..21285258hg19UCSC Ensembl
Outerchr13:21284487..21285275hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550134
Supporting Variants
Samples
Known GenesIL17D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9748881
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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