A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977356



Internal ID16271312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162136930..162227323hg38UCSC Ensembl
Innerchr3:161854718..161945111hg19UCSC Ensembl
Innerchr3:163337412..163427805hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3890394
hg1990394
hg1890394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592147
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv977356
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