A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522842



Internal ID15103449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27522789..27685343hg38UCSC Ensembl
Innerchr1:27849300..28011854hg19UCSC Ensembl
Innerchr1:27721887..27884441hg18UCSC Ensembl
Innerchr1:27533442..27695996hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38162555
hg19162555
hg18162555
hg17162555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698494
Samples
Known GenesAHDC1, FGR, IFI6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522842
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