A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16474755



Internal ID19338315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94203393..94203393hg38UCSC Ensembl
chr9:96965675..96965675hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3650613
Supporting Variants
Samples
Known GenesMIRLET7DHG
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)essv16474755
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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