A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571100



Internal ID16011823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1060644..1109731hg38UCSC Ensembl
Innerchr16:1110644..1159731hg19UCSC Ensembl
Innerchr16:1050645..1099732hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3849088
hg1949088
hg1849088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149289
SamplesHGDP01223
Known GenesC1QTNF8, SSTR5, SSTR5-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571100
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