A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694691



Internal ID15084657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3391470..3398032hg38UCSC Ensembl
Innerchr1:3308034..3314596hg19UCSC Ensembl
Innerchr1:3297894..3304456hg18UCSC Ensembl
Innerchr1:3331191..3337753hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg386563
hg196563
hg186563
hg176563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521921
Supporting Variants
Samples
Known GenesPRDM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694691
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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