A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607408



Internal ID16048131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66125574..66134209hg38UCSC Ensembl
Innerchr7:65590561..65599196hg19UCSC Ensembl
Innerchr7:65227996..65236631hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg388636
hg198636
hg188636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11433n54
Supporting Variantsnssv1085672
Samples
Known GenesCRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607408
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