A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148893



Internal ID15506864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1729694..1789022hg38UCSC Ensembl
Innerchr16:1779695..1839023hg19UCSC Ensembl
Innerchr16:1719696..1779024hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3859329
hg1959329
hg1859329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571169
Supporting Variants
Samples1780854288_A
Known GenesEME2, MAPK8IP3, MIR3177, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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