A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034818



Internal ID19124039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..366333hg38UCSC Ensembl
Innerchr6:302294..366333hg19UCSC Ensembl
Innerchr6:247294..311333hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3864040
hg1964040
hg1864040
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5891n100
Supporting Variantsnssv3653733, nssv3747830, nssv3653727, nssv3653730, nssv3653729, nssv3747831, nssv3653732, nssv3653731, nssv3747829, nssv3653728, nssv3653734, nssv3653726, nssv3747832
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034818
Frequency
Sample Size11257
Observed Gain12
Observed Loss1
Observed Complex0
Frequencyn/a


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