A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3651482



Internal ID18949763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..302294hg38UCSC Ensembl
Innerchr6:257341..302294hg19UCSC Ensembl
Innerchr6:202341..247294hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3844954
hg1944954
hg1844954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018010
Supporting Variants
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)nssv3651482
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