A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083667



Internal ID15590167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45078310..45080649hg38UCSC Ensembl
Innerchr7:45117909..45120248hg19UCSC Ensembl
Innerchr7:45084434..45086773hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606846
Supporting Variants
Samples
Known GenesNACAD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083667
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