A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019729



Internal ID19108947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13176688..13226060hg38UCSC Ensembl
Innerchr8:13034197..13083569hg19UCSC Ensembl
Innerchr8:13078568..13127940hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3849373
hg1949373
hg1849373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7085n100
Supporting Variantsnssv3666987
Samples
Known GenesDLC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019729
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