A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016306



Internal ID19105525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36566134..36622783hg38UCSC Ensembl
Innerchr8:36423652..36480301hg19UCSC Ensembl
Innerchr8:36542810..36599459hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3856650
hg1956650
hg1856650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7161n100
Supporting Variantsnssv3760501
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)nsv1016306
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