A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054064



Internal ID19143283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77171313hg38UCSC Ensembl
Innerchr9:79770398..79786229hg19UCSC Ensembl
Innerchr9:78960218..78976049hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3815832
hg1915832
hg1815832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3759773
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)nsv1054064
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