A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009857



Internal ID19099076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68647189..68697283hg38UCSC Ensembl
Innerchr3:68696340..68746434hg19UCSC Ensembl
Innerchr3:68779030..68829124hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3850095
hg1950095
hg1850095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593978
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)nsv1009857
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