A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018671



Internal ID19107888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8102490..8163549hg38UCSC Ensembl
Innerchr9:8102490..8163549hg19UCSC Ensembl
Innerchr9:8092490..8153549hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3861060
hg1961060
hg1861060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7395n100
Supporting Variantsnssv3689117
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)nsv1018671
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