A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019020



Internal ID19108237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326413..40339978hg38UCSC Ensembl
Innerchr8:40183932..40197497hg19UCSC Ensembl
Innerchr8:40303089..40316654hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3813566
hg1913566
hg1813566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7184n100
Supporting Variantsnssv3687237
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)nsv1019020
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