A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058826



Internal ID15565326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49463856..49478796hg38UCSC Ensembl
Innerchr6:49431569..49446509hg19UCSC Ensembl
Innerchr6:49539528..49554468hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3814941
hg1914941
hg1814941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603089
Supporting Variants
Samples
Known GenesCENPQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058826
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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