A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511665



Internal ID15851090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:55676243..55678643hg38UCSC Ensembl
OuterchrX:55660407..55711827hg38UCSC Ensembl
InnerchrX:55702676..55705076hg19UCSC Ensembl
OuterchrX:55686840..55738260hg19UCSC Ensembl
InnerchrX:55719401..55721801hg18UCSC Ensembl
OuterchrX:55703565..55754985hg18UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3851421
hg1951421
hg1851421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626302
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)nsv511665
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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