A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591851



Internal ID16379260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136504112..136706758hg38UCSC Ensembl
Innerchr3:136222954..136425600hg19UCSC Ensembl
Innerchr3:137705644..137908290hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38202647
hg19202647
hg18202647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152540
Samples1780862484_A
Known GenesSTAG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591851
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