A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051015



Internal ID19140234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53526266..53551719hg38UCSC Ensembl
Innerchr13:54100401..54125854hg19UCSC Ensembl
Innerchr13:52998402..53023855hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3825454
hg1925454
hg1825454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523477
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)nsv1051015
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