A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611749



Internal ID16399158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94433277..94435179hg38UCSC Ensembl
Innerchr8:95445505..95447407hg19UCSC Ensembl
Innerchr8:95514681..95516583hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381903
hg191903
hg181903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117842
Samples
Known GenesFSBP, RAD54B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611749
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