A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600837



Internal ID18899118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33989883..34013910hg38UCSC Ensembl
Innerchr22:34385872..34409899hg19UCSC Ensembl
Innerchr22:32715872..32739899hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3824028
hg1924028
hg1824028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065150
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600837
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