A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592619



Internal ID16380028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177576293..177578979hg38UCSC Ensembl
Innerchr3:177294081..177296767hg19UCSC Ensembl
Innerchr3:178776775..178779461hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382687
hg192687
hg182687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8751n54
Supporting Variantsnssv981627
Samples
Known GenesLINC00578
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592619
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