A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011923



Internal ID18754459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44522..244340hg38UCSC Ensembl
Innerchr3:86204..286023hg19UCSC Ensembl
Innerchr3:61204..261023hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38199819
hg19199820
hg18199820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4607n100
Supporting Variantsnssv3590257
Samples
Known GenesCHL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011923
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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