A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522089



Internal ID15102696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141840747..141876963hg38UCSC Ensembl
InnerchrX:140928533..140964749hg19UCSC Ensembl
InnerchrX:140756199..140792415hg18UCSC Ensembl
InnerchrX:140654053..140690269hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3836217
hg1936217
hg1836217
hg1736217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694861
Samples
Known GenesMAGEC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522089
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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