A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3667469



Internal ID19385477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1605561..1606213hg38UCSC Ensembl
chr1:1540941..1541593hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16489926
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)esv3667469
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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