A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703539



Internal ID15093505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171329801..171331209hg38UCSC Ensembl
Innerchr1:171298940..171300348hg19UCSC Ensembl
Innerchr1:169565564..169566972hg18UCSC Ensembl
Innerchr1:168030598..168032006hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg381409
hg191409
hg181409
hg171409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527149
Supporting Variants
Samples
Known GenesFMO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703539
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