A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012746



Internal ID19101963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23640405..23715661hg38UCSC Ensembl
Innerchr4:23642028..23717284hg19UCSC Ensembl
Innerchr4:23251126..23326382hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3875257
hg1975257
hg1875257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5156n100
Supporting Variantsnssv3620585
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)nsv1012746
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