A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046109



Internal ID19135328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77171524hg38UCSC Ensembl
Innerchr9:79770398..79786440hg19UCSC Ensembl
Innerchr9:78960218..78976260hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3816043
hg1916043
hg1816043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3696383
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)nsv1046109
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