A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv516n21



Internal ID20132237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71666911..71890381hg38UCSC Ensembl
chrX:70886761..71110231hg19UCSC Ensembl
chrX:70803486..71026956hg18UCSC Ensembl
chrX:70669782..70893252hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38223471
hg19223471
hg18223471
hg17223471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523166, nsv520952
Samples
Known GenesBCYRN1, CXorf49, CXorf49B, LINC00891, LOC100132741
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv516n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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