A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604458



Internal ID16391867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108289570..108291863hg38UCSC Ensembl
Innerchr6:108610774..108613067hg19UCSC Ensembl
Innerchr6:108717467..108719760hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382294
hg192294
hg182294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10900n54
Supporting Variantsnssv1071909
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604458
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