A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847692



Internal ID15794962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84887769..84905644hg38UCSC Ensembl
Innerchr15:85431000..85448875hg19UCSC Ensembl
Innerchr15:83232004..83249879hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3817876
hg1917876
hg1817876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570289
Supporting Variants
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv847692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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