A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589741



Internal ID16377150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13637835..13640055hg38UCSC Ensembl
Innerchr3:13679335..13681555hg19UCSC Ensembl
Innerchr3:13654336..13656556hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382221
hg192221
hg182221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8231n54
Supporting Variantsnssv959226
Samples
Known GenesFBLN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589741
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