A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046582



Internal ID19135801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42671626..42718605hg38UCSC Ensembl
Innerchr10:43167074..43214053hg19UCSC Ensembl
Innerchr10:42487080..42534059hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3846980
hg1946980
hg1846980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509019
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)nsv1046582
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