A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571549



Internal ID16012272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16152307..16167394hg38UCSC Ensembl
Innerchr16:16246164..16261251hg19UCSC Ensembl
Innerchr16:16153665..16168752hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3815088
hg1915088
hg1815088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4927n54
Supporting Variantsnssv852824, nssv852827, nssv852825, nssv852826
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571549
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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