A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608234



Internal ID16048957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114432388..114507162hg38UCSC Ensembl
Innerchr7:114072443..114147217hg19UCSC Ensembl
Innerchr7:113859679..113934453hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3874775
hg1974775
hg1874775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11584n54
Supporting Variantsnssv1092753
Samples
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608234
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