A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511651



Internal ID15851076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:67904034..67907640hg38UCSC Ensembl
OuterchrX:67878232..67907735hg38UCSC Ensembl
InnerchrX:67123876..67127482hg19UCSC Ensembl
OuterchrX:67098074..67127577hg19UCSC Ensembl
InnerchrX:67040601..67044207hg18UCSC Ensembl
OuterchrX:67014799..67044302hg18UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3829504
hg1929504
hg1829504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626286
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511651
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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