A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3661578



Internal ID19032900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38659172..38659172hg38UCSC Ensembl
chr22:39055177..39055177hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16484623
Samples
Known GenesCBY1
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)esv3661578
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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