A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3674279



Internal ID19392287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63128879..63140631hg38UCSC Ensembl
chrX:62348349..62360099hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3811753
hg1911751
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16496055
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)esv3674279
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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