A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv63n50



Internal ID20133421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157255..49162942hg38UCSC Ensembl
chrX:49013637..49019347hg19UCSC Ensembl
chrX:48900581..48906291hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385688
hg195711
hg185711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513725, nsv513724
Samples1
Known GenesMAGIX
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv63n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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