A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053872



Internal ID19143091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61309281..61325124hg38UCSC Ensembl
Innerchr15:61601480..61617323hg19UCSC Ensembl
Innerchr15:59388772..59404615hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3815844
hg1915844
hg1815844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553630
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)nsv1053872
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