A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3676855



Internal ID19394863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:866474..866532hg38UCSC Ensembl
chr7:906111..906169hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16498373
Samples
Known GenesSUN1
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)esv3676855
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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