A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16465566



Internal ID19329126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22834692..22834787hg38UCSC Ensembl
chr20:22815330..22815425hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3663052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)essv16465566
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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