A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3672702



Internal ID19390710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75839700..75839716hg38UCSC Ensembl
chr10:77599458..77599474hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3817
hg1917
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16494635
Samples
Known GenesC10orf11
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)esv3672702
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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