A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513725



Internal ID15853146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49157255..49162817hg38UCSC Ensembl
OuterchrX:49013762..49019347hg19UCSC Ensembl
OuterchrX:48900706..48906291hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385563
hg195586
hg185586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n50
Supporting Variantsnssv626977
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)nsv513725
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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