A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555100



Internal ID18853381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87242912..87327490hg38UCSC Ensembl
Innerchr15:87786143..87870721hg19UCSC Ensembl
Innerchr15:85587147..85671725hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3884579
hg1984579
hg1884579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053454
Supporting Variants
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)nssv3555100
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