A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3668664



Internal ID19039986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124809372..124809372hg38UCSC Ensembl
chr10:126497941..126497941hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16491001
Samples
Known GenesFAM175B
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)esv3668664
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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