A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511659



Internal ID15851084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30793429..30806915hg38UCSC Ensembl
OuterchrX:30772765..30811227hg38UCSC Ensembl
InnerchrX:30811546..30825032hg19UCSC Ensembl
OuterchrX:30790882..30829344hg19UCSC Ensembl
InnerchrX:30721467..30734953hg18UCSC Ensembl
OuterchrX:30700803..30739265hg18UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3838463
hg1938463
hg1838463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626295
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)nsv511659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer