A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526304



Internal ID15453597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31241120..31263704hg38UCSC Ensembl
InnerchrX:31259237..31281821hg19UCSC Ensembl
InnerchrX:31169158..31191742hg18UCSC Ensembl
InnerchrX: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 Variantsdgv506n21
Supporting Variantsnssv702586
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526304
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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