A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156601



Internal ID15526906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43269523..43936548hg38UCSC Ensembl
Innerchr8:43124666..43791691hg19UCSC Ensembl
Innerchr8:43243823..43910848hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38667026
hg19667026
hg18667026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611149
Supporting Variants
SamplesHGDP00258
Known GenesPOTEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156601
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