A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3674455



Internal ID19392463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18170229..18188593hg38UCSC Ensembl
chrY:20332115..20350479hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3818365
hg1918365
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16496213
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)esv3674455
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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