A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716722



Internal ID18668317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46672048..46758543hg38UCSC Ensembl
Innerchr15:46964246..47050741hg19UCSC Ensembl
Innerchr15:44751538..44838033hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3886496
hg1986496
hg1886496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050429
Supporting Variants
Samples
Known GenesMIR548A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716722
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