A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033626



Internal ID19122847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:290586..385772hg38UCSC Ensembl
Innerchr6:290586..385772hg19UCSC Ensembl
Innerchr6:235586..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3895187
hg1995187
hg1895187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5888n100
Supporting Variantsnssv3653703
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)nsv1033626
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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