A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030098



Internal ID19119317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:267610..355524hg38UCSC Ensembl
Innerchr6:267610..355524hg19UCSC Ensembl
Innerchr6:212610..300524hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3887915
hg1987915
hg1887915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3653633
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)nsv1030098
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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