A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151886



Internal ID15854603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15651452..15733318hg38UCSC Ensembl
Innerchr3:15692959..15774825hg19UCSC Ensembl
Innerchr3:15667963..15749829hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3881867
hg1981867
hg1881867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589781
Supporting Variants
Samples1780862226_A
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151886
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