A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026935



Internal ID19116153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:249798..336797hg38UCSC Ensembl
Innerchr6:249798..336797hg19UCSC Ensembl
Innerchr6:194798..281797hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3887000
hg1987000
hg1887000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3650387, nssv3650388
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)nsv1026935
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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