A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022831



Internal ID18765365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79748262..79809658hg38UCSC Ensembl
Innerchr8:80660497..80721893hg19UCSC Ensembl
Innerchr8:80823052..80884448hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3861397
hg1961397
hg1861397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7245n100
Supporting Variantsnssv3689587
Samples
Known GenesHEY1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022831
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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