A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3674903



Internal ID19392911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1812215..1812366hg38UCSC Ensembl
chr4:1813942..1814093hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16496616
Samples
Known GenesLETM1
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)esv3674903
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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