A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023834



Internal ID19113051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9940562..10047278hg38UCSC Ensembl
Innerchr8:9798072..9904788hg19UCSC Ensembl
Innerchr8:9835482..9942198hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38106717
hg19106717
hg18106717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681709
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)nsv1023834
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