A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520777



Internal ID15448070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:153002821..153008873hg38UCSC Ensembl
InnerchrX:152171365..152177417hg19UCSC Ensembl
InnerchrX:151922021..151928073hg18UCSC Ensembl
InnerchrX:151841933..151847985hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386053
hg196053
hg186053
hg176053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675289, nssv686888
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520777
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer