A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016608



Internal ID19105827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133151196..133168229hg38UCSC Ensembl
Innerchr8:134163440..134180473hg19UCSC Ensembl
Innerchr8:134232622..134249655hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3817034
hg1917034
hg1817034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7322n100
Supporting Variantsnssv3691576
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer