A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852069



Internal ID15799339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1764390..1817039hg38UCSC Ensembl
Innerchr16:1814391..1867040hg19UCSC Ensembl
Innerchr16:1754392..1807041hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3852650
hg1952650
hg1852650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571172
Supporting Variants
Samples
Known GenesEME2, HAGH, IGFALS, MAPK8IP3, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852069
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