A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589893



Internal ID16377302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21217943..21316760hg38UCSC Ensembl
Innerchr3:21259435..21358252hg19UCSC Ensembl
Innerchr3:21234439..21333256hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3898818
hg1998818
hg1898818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv959917
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589893
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