A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516080



Internal ID15443373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:35091453..35099121hg38UCSC Ensembl
InnerchrX:35109570..35117238hg19UCSC Ensembl
InnerchrX:35019491..35027159hg18UCSC Ensembl
InnerchrX:34869227..34876895hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg387669
hg197669
hg187669
hg177669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671507, nssv668768, nssv666063
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516080
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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