A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153445



Internal ID15876936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12359578..12382323hg38UCSC Ensembl
Innerchr4:12361202..12383947hg19UCSC Ensembl
Innerchr4:11970300..11993045hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3822746
hg1922746
hg1822746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593746
Supporting Variants
SamplesHGDP00914
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153445
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