A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034877



Internal ID19124097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114248041..114280691hg38UCSC Ensembl
Innerchr8:115260270..115292920hg19UCSC Ensembl
Innerchr8:115329446..115362096hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3832651
hg1932651
hg1832651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7289n100
Supporting Variantsnssv3691320, nssv3757345
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)nsv1034877
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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