A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999236



Internal ID18812086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65736202..65891404hg38UCSC Ensembl
Innerchr3:65721877..65877079hg19UCSC Ensembl
Innerchr3:65696917..65852119hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38155203
hg19155203
hg18155203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4769n100
Supporting Variantsnssv3593959
Samples
Known GenesMAGI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999236
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer