A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626289



Internal ID15849822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123238802..123239465hg38UCSC Ensembl
OuterchrX:123235466..123246769hg38UCSC Ensembl
InnerchrX:122372653..122373316hg19UCSC Ensembl
OuterchrX:122369317..122380620hg19UCSC Ensembl
InnerchrX:122200334..122200997hg18UCSC Ensembl
OuterchrX:122196998..122208301hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3811304
hg1911304
hg1811304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511653
Supporting Variants
Samples1
Known GenesGRIA3
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626289
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