A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1043278



Internal ID15549778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:148825809..148826877hg38UCSC Ensembl
Innerchr5:148205372..148206440hg19UCSC Ensembl
Innerchr5:148185565..148186633hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381069
hg191069
hg181069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599947
Supporting Variants
Samples
Known GenesADRB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1043278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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