A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030620



Internal ID19119839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..381137hg38UCSC Ensembl
Innerchr6:264744..381137hg19UCSC Ensembl
Innerchr6:209744..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38116394
hg19116394
hg18116394
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3747789, nssv3653590, nssv3653579, nssv3653576, nssv3653592, nssv3653594, nssv3653587, nssv3653580, nssv3653575, nssv3653591, nssv3653589, nssv3747791, nssv3653583, nssv3747788, nssv3747790, nssv3653578, nssv3653582, nssv3747787, nssv3653581, nssv3653593, nssv3653595, nssv3653586, nssv3747792, nssv3653588, nssv3653577, nssv3653585, nssv3653584, nssv3653574, nssv3653596
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)nsv1030620
Frequency
Sample Size11257
Observed Gain9
Observed Loss20
Observed Complex0
Frequencyn/a


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