A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591976



Internal ID16379385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149232993..149251541hg38UCSC Ensembl
Innerchr3:148950780..148969328hg19UCSC Ensembl
Innerchr3:150433470..150452018hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3818549
hg1918549
hg1818549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8637n54
Supporting Variantsnssv976388
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591976
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