A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521559



Internal ID15448852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142259520..142282326hg38UCSC Ensembl
InnerchrX:141347306..141370112hg19UCSC Ensembl
InnerchrX:141174972..141197778hg18UCSC Ensembl
InnerchrX:141072826..141095632hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3822807
hg1922807
hg1822807
hg1722807
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv534n21
Supporting Variantsnssv698174
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521559
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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