A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522479



Internal ID15449772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45445285..45515289hg38UCSC Ensembl
InnerchrX:45304530..45374534hg19UCSC Ensembl
InnerchrX:45189474..45259478hg18UCSC Ensembl
InnerchrX:45060784..45130788hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3870005
hg1970005
hg1870005
hg1770005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705845
Samples
Known GenesLOC101927528
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522479
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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