A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521510



Internal ID15102117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31213555..31236885hg38UCSC Ensembl
InnerchrX:31231672..31255002hg19UCSC Ensembl
InnerchrX:31141593..31164923hg18UCSC Ensembl
InnerchrX:30991329..31014659hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3823331
hg1923331
hg1823331
hg1723331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698127
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521510
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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