A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16476151



Internal ID18993025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122456297..122456297hg38UCSC Ensembl
chr10:124215813..124215813hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3652164
Supporting Variants
Samples
Known GenesARMS2
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)essv16476151
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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