A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036453



Internal ID19125672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63754886..63855900hg38UCSC Ensembl
Innerchr13:64329019..64430033hg19UCSC Ensembl
Innerchr13:63227020..63328034hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38101015
hg19101015
hg18101015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n100
Supporting Variantsnssv3526738
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)nsv1036453
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