A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512666



Internal ID15852091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3785091..3793307hg38UCSC Ensembl
OuterchrX:3703132..3711348hg19UCSC Ensembl
OuterchrX:3713132..3721348hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg388217
hg198217
hg188217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625285
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512666
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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