A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590459



Internal ID16031182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63654925..63687658hg38UCSC Ensembl
Innerchr3:63640601..63673334hg19UCSC Ensembl
Innerchr3:63615641..63648374hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3832734
hg1932734
hg1832734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151909
SamplesNINDS_112
Known GenesSNTN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590459
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