A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591994



Internal ID16379403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149245608..149270366hg38UCSC Ensembl
Innerchr3:148963395..148988153hg19UCSC Ensembl
Innerchr3:150446085..150470843hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3824759
hg1924759
hg1824759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976492
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591994
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