A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521797



Internal ID15449090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31724129..32114213hg38UCSC Ensembl
InnerchrX:31742246..32132330hg19UCSC Ensembl
InnerchrX:31652167..32042251hg18UCSC Ensembl
InnerchrX:31501903..31891987hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38390085
hg19390085
hg18390085
hg17390085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694567
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521797
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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