A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611045



Internal ID16398454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39406879..39487454hg38UCSC Ensembl
Innerchr8:39264398..39344973hg19UCSC Ensembl
Innerchr8:39383555..39464130hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3880576
hg1980576
hg1880576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12103n54
Supporting Variantsnssv1111181
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611045
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