A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033008



Internal ID19122230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:237215..350608hg38UCSC Ensembl
Innerchr6:237215..350608hg19UCSC Ensembl
Innerchr6:182215..295608hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38113394
hg19113394
hg18113394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3650381
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)nsv1033008
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