A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013972



Internal ID19103191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99225602..99279362hg38UCSC Ensembl
Innerchr3:98944446..98998206hg19UCSC Ensembl
Innerchr3:100427136..100480896hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3853761
hg1953761
hg1853761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4828n100
Supporting Variantsnssv3604226
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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