A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605690



Internal ID16046413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:551684..552261hg38UCSC Ensembl
Innerchr7:591321..591898hg19UCSC Ensembl
Innerchr7:557847..558424hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38578
hg19578
hg18578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11108n54
Supporting Variantsnssv1077799
Samples
Known GenesPRKAR1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605690
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