A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591204



Internal ID16378613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103805473..103869582hg38UCSC Ensembl
Innerchr3:103524317..103588426hg19UCSC Ensembl
Innerchr3:105007007..105071116hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3864110
hg1964110
hg1864110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152510
SamplesNINDS_162
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591204
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