A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018578



Internal ID19107795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67630488..67644593hg38UCSC Ensembl
Innerchr8:68542723..68556828hg19UCSC Ensembl
Innerchr8:68705277..68719382hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3814106
hg1914106
hg1814106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7236n100
Supporting Variantsnssv3689490, nssv3689491, nssv3689492, nssv3689489
Samples
Known GenesCPA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018578
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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