A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16470171



Internal ID18987045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56348113..56348194hg38UCSC Ensembl
chr12:56741897..56741978hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3685660
Supporting Variants
Samples
Known GenesSTAT2
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)essv16470171
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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