A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521673



Internal ID15448966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29270532..29415237hg38UCSC Ensembl
InnerchrX:29288649..29433354hg19UCSC Ensembl
InnerchrX:29198570..29343275hg18UCSC Ensembl
InnerchrX:29048306..29193011hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38144706
hg19144706
hg18144706
hg17144706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698291
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521673
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