A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512693



Internal ID15852118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115307609..115310301hg38UCSC Ensembl
OuterchrX:114542174..114544866hg19UCSC Ensembl
OuterchrX:114448430..114451122hg18UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382693
hg192693
hg182693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n50
Supporting Variantsnssv625315
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)nsv512693
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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