A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603350



Internal ID16390759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62356335..62442819hg38UCSC Ensembl
Innerchr6:63066240..63152724hg19UCSC Ensembl
Innerchr6:63124199..63210683hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3886485
hg1986485
hg1886485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10711n54
Supporting Variantsnssv1061235
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603350
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