A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3652754



Internal ID18951035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..379003hg38UCSC Ensembl
Innerchr6:260364..379003hg19UCSC Ensembl
Innerchr6:205364..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38118640
hg19118640
hg18118640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033119
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)nssv3652754
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