A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047163



Internal ID18789694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77175148hg38UCSC Ensembl
Innerchr9:79770398..79790064hg19UCSC Ensembl
Innerchr9:78960218..78979884hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3819667
hg1919667
hg1819667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7682n100
Supporting Variantsnssv3696391, nssv3696392
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)nsv1047163
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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