A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590122



Internal ID16377531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41318043..41783064hg38UCSC Ensembl
Innerchr3:41359534..41824556hg19UCSC Ensembl
Innerchr3:41334538..41799560hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38465022
hg19465023
hg18465023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8290n54
Supporting Variantsnssv962399
Samples
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590122
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