A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571277



Internal ID16358686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4315234..4316611hg38UCSC Ensembl
Innerchr16:4365235..4366612hg19UCSC Ensembl
Innerchr16:4305236..4306613hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381378
hg191378
hg181378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4880n54
Supporting Variantsnssv852304, nssv852305
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571277
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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