A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755981



Internal ID18730227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56175888..56179832hg38UCSC Ensembl
Outerchr20:56175327..56179944hg38UCSC Ensembl
Innerchr20:54750944..54754888hg19UCSC Ensembl
Outerchr20:54750383..54755000hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384618
hg194618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755981
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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