A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023546



Internal ID19112763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8151670..8277205hg38UCSC Ensembl
Innerchr8:8009192..8134727hg19UCSC Ensembl
Innerchr8:8046602..8172137hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38125536
hg19125536
hg18125536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7000n100
Supporting Variantsnssv3681636
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023546
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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