A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511669



Internal ID15851094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97602569..97655550hg38UCSC Ensembl
OuterchrX:97599971..97671552hg38UCSC Ensembl
InnerchrX:96857568..96910549hg19UCSC Ensembl
OuterchrX:96854970..96926551hg19UCSC Ensembl
InnerchrX:96744224..96797205hg18UCSC Ensembl
OuterchrX:96741626..96813207hg18UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3871582
hg1971582
hg1871582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv64n50
Supporting Variantsnssv626306
Samples1
Known GenesDIAPH2
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511669
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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