A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032314



Internal ID18774848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:175479..328345hg38UCSC Ensembl
Innerchr6:175479..328345hg19UCSC Ensembl
Innerchr6:120479..273345hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38152867
hg19152867
hg18152867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5868n100
Supporting Variantsnssv3746765
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)nsv1032314
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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