A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv537n21



Internal ID22766729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145250160..145384001hg38UCSC Ensembl
chrX:144331680..144465519hg19UCSC Ensembl
chrX:144139372..144273211hg18UCSC Ensembl
chrX:144037226..144171065hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38133842
hg19133840
hg18133840
hg17133840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518796, nsv527680
Samples
Known GenesSPANXN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv537n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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