A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851938



Internal ID15799208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1078406..1287716hg38UCSC Ensembl
Innerchr16:1128406..1337717hg19UCSC Ensembl
Innerchr16:1068407..1277718hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38209311
hg19209312
hg18209312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571101
Supporting Variants
Samples
Known GenesC1QTNF8, CACNA1H, SSTR5, SSTR5-AS1, TPSAB1, TPSB2, TPSD1, TPSG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851938
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer