A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16496228



Internal ID19359788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:25662878..25667676hg38UCSC Ensembl
chrY:27809025..27813823hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg384799
hg194799
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3674471
Supporting Variants
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)essv16496228
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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