A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054906



Internal ID19144125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22109020..22186960hg38UCSC Ensembl
Innerchr13:22683159..22761099hg19UCSC Ensembl
Innerchr13:21581159..21659099hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3877941
hg1977941
hg1877941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714944
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)nsv1054906
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