A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003589



Internal ID19092807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5335093..5379399hg38UCSC Ensembl
Innerchr2:5475226..5519532hg19UCSC Ensembl
Innerchr2:5392677..5436983hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3844307
hg1944307
hg1844307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3710n100
Supporting Variantsnssv3576927
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)nsv1003589
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