A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611449



Internal ID16052172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:64598475..64630844hg38UCSC Ensembl
Innerchr8:65511032..65543401hg19UCSC Ensembl
Innerchr8:65673586..65705955hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3832370
hg1932370
hg1832370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115725
Samples
Known GenesCYP7B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611449
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