A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16478162



Internal ID18995036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116866390..116866390hg38UCSC Ensembl
chr12:117304195..117304195hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3654398
Supporting Variants
Samples
Known GenesHRK
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)essv16478162
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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