A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv64n50



Internal ID22767893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97599971..97671552hg38UCSC Ensembl
chrX:96854970..96926551hg19UCSC Ensembl
chrX: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 Variants
Supporting Variantsnsv512692, nsv511669
Samples1
Known GenesDIAPH2
MethodSequencing
SNP array
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Not reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv64n50
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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