A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16474526



Internal ID19338086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32524596..32524596hg38UCSC Ensembl
chr9:32524594..32524594hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3650359
Supporting Variants
Samples
Known GenesDDX58
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)essv16474526
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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