A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3672302



Internal ID19390310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61438646..61438647hg38UCSC Ensembl
chr8:62351205..62351206hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16494276
Samples
Known GenesCLVS1
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)esv3672302
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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