A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863581



Internal ID15810851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89851129..89852597hg38UCSC Ensembl
Innerchr16:89917537..89919005hg19UCSC Ensembl
Innerchr16:88445038..88446506hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381469
hg191469
hg181469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573789
Supporting Variants
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863581
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