A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16464561



Internal ID18981435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135563168..135563324hg38UCSC Ensembl
chr9:138455014..138455170hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3651886
Supporting Variants
Samples
Known GenesPAEP
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)essv16464561
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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