A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611634



Internal ID16399043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83244363..83367649hg38UCSC Ensembl
Innerchr8:84156598..84279884hg19UCSC Ensembl
Innerchr8:84319153..84442439hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38123287
hg19123287
hg18123287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12217n54
Supporting Variantsnssv1117328
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611634
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