A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021626



Internal ID19110844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:285695..381137hg38UCSC Ensembl
Innerchr6:285695..381137hg19UCSC Ensembl
Innerchr6:230695..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3895443
hg1995443
hg1895443
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5890n100
Supporting Variantsnssv3653679, nssv3747809, nssv3653678, nssv3653682, nssv3653680, nssv3747808, nssv3653686, nssv3747807, nssv3653685, nssv3653681, nssv3653683, nssv3653684, nssv3653687
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)nsv1021626
Frequency
Sample Size11257
Observed Gain3
Observed Loss10
Observed Complex0
Frequencyn/a


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