A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973136



Internal ID15920406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129357694..129389806hg38UCSC Ensembl
Innerchr3:129076537..129108649hg19UCSC Ensembl
Innerchr3:130559227..130591339hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3832113
hg1932113
hg1832113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591658
Supporting Variants
Samples
Known GenesRPL32P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv973136
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