A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511668



Internal ID15504407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:77866198..77868048hg38UCSC Ensembl
OuterchrX:77850548..77905037hg38UCSC Ensembl
InnerchrX:77121695..77123545hg19UCSC Ensembl
OuterchrX:77106045..77160534hg19UCSC Ensembl
InnerchrX:77008351..77010201hg18UCSC Ensembl
OuterchrX:76992701..77047190hg18UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3854490
hg1954490
hg1854490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626305
Samples1
Known GenesCOX7B, MAGT1
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511668
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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