A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521731



Internal ID15449024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30098536..30119163hg38UCSC Ensembl
InnerchrX:30116653..30137280hg19UCSC Ensembl
InnerchrX:30026574..30047201hg18UCSC Ensembl
InnerchrX:29876310..29896937hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3820628
hg1920628
hg1820628
hg1720628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521731
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