A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591908



Internal ID16032631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141876606..141877120hg38UCSC Ensembl
Innerchr3:141595448..141595962hg19UCSC Ensembl
Innerchr3:143078138..143078652hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38515
hg19515
hg18515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8624n54
Supporting Variantsnssv975203
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591908
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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