A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847253



Internal ID16141209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77495127..77559193hg38UCSC Ensembl
Innerchr15:77787469..77851535hg19UCSC Ensembl
Innerchr15:75574524..75638590hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3864067
hg1964067
hg1864067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570140
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv847253
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