A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16482506



Internal ID19346066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24184673..24184673hg38UCSC Ensembl
chr2:24407542..24407542hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3659225
Supporting Variants
Samples
Known GenesFAM228A
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)essv16482506
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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