A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042239



Internal ID19131458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18600494..18737640hg38UCSC Ensembl
Innerchr13:19174634..19311780hg19UCSC Ensembl
Innerchr13:18072634..18209780hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38137147
hg19137147
hg18137147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1604n100
Supporting Variantsnssv3714929
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)nsv1042239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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