A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv506n21



Internal ID22766698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31241120..31263704hg38UCSC Ensembl
chrX:31259237..31281821hg19UCSC Ensembl
chrX:31169158..31191742hg18UCSC Ensembl
chrX:31018894..31041478hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3822585
hg1922585
hg1822585
hg1722585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523957, nsv526304
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv506n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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