A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590806



Internal ID16378215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82874210..82973236hg38UCSC Ensembl
Innerchr3:82923361..83022387hg19UCSC Ensembl
Innerchr3:83006051..83105077hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3899027
hg1999027
hg1899027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8410n54
Supporting Variantsnssv967068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590806
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