A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153462



Internal ID15876741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62171606..62292842hg38UCSC Ensembl
Innerchr4:63037324..63158560hg19UCSC Ensembl
Innerchr4:62719919..62841155hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38121237
hg19121237
hg18121237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594334
Supporting Variants
SamplesHGDP00886
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153462
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