A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16501766



Internal ID19018640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47779761..47779876hg38UCSC Ensembl
chr8:48692322..48692437hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3680624
Supporting Variants
Samples
Known GenesPRKDC
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)essv16501766
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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