A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611846



Internal ID16052569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106766096..106807140hg38UCSC Ensembl
Innerchr8:107778324..107819368hg19UCSC Ensembl
Innerchr8:107847500..107888544hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3841045
hg1941045
hg1841045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118241
Samples
Known GenesABRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611846
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