A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512676



Internal ID15852101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55675553..55684854hg38UCSC Ensembl
OuterchrX:55701986..55711287hg19UCSC Ensembl
OuterchrX:55718711..55728012hg18UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg389302
hg199302
hg189302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625296
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)nsv512676
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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