A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049107



Internal ID19138326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104772904..104797192hg38UCSC Ensembl
Innerchr13:105425255..105449543hg19UCSC Ensembl
Innerchr13:104223256..104247544hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3824289
hg1924289
hg1824289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n100
Supporting Variantsnssv3525553
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)nsv1049107
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