A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv62n50



Internal ID11602377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46951443..46971306hg38UCSC Ensembl
chrX:46810554..46831299hg19UCSC Ensembl
chrX:46695498..46716243hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819864
hg1920746
hg1820746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv513723, nsv513722
Samples1
Known GenesJADE3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv62n50
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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