A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv62n50



Internal ID6316189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46810554..46831299hg19UCSC Ensembl
chrX:46695498..46716243hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeOTHER Inversion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv513723, nsv513722
Samples1
Known GenesPHF16
Method
Analysis
Platform
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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