A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152229



Internal ID15526498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143598..212269hg38UCSC Ensembl
Innerchr3:185281..253952hg19UCSC Ensembl
Innerchr3:160281..228952hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3868672
hg1968672
hg1868672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589246
Supporting Variants
SamplesHGDP00140
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152229
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