A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755629



Internal ID18729875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16241163..16241638hg38UCSC Ensembl
Outerchr20:16241049..16241753hg38UCSC Ensembl
Innerchr20:16221808..16222283hg19UCSC Ensembl
Outerchr20:16221694..16222398hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755629
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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