A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16486918



Internal ID19003792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239894299..239894299hg38UCSC Ensembl
chr2:240833716..240833716hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3664127
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)essv16486918
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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