A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3687932



Internal ID19405940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77977679..77977739hg38UCSC Ensembl
chr13:78551814..78551874hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16472216
Samples
Known Genes
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)esv3687932
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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