A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552339



Internal ID18503934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44804341..44937386hg38UCSC Ensembl
Innerchr15:45096539..45229584hg19UCSC Ensembl
Innerchr15:42883831..43016876hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38133046
hg19133046
hg18133046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050650
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)nssv3552339
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer