A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572360



Internal ID16359769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34961511hg38UCSC Ensembl
Innerchr16:34173678..34195882hg19UCSC Ensembl
Innerchr16:34031179..34053383hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3822228
hg1922205
hg1822205
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5081n54
Supporting Variantsnssv856208, nssv856209
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572360
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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