A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602990



Internal ID16043713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42085013..42130449hg38UCSC Ensembl
Innerchr6:42052751..42098187hg19UCSC Ensembl
Innerchr6:42160729..42206165hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3845437
hg1945437
hg1845437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10639n54
Supporting Variantsnssv1153692
SamplesNINDS_70
Known GenesC6orf132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602990
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