A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028083



Internal ID19117301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95435558..95446966hg38UCSC Ensembl
Innerchr8:96447786..96459194hg19UCSC Ensembl
Innerchr8:96516962..96528370hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811409
hg1911409
hg1811409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7274n100
Supporting Variantsnssv3689735
Samples
Known GenesLOC100616530
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028083
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