A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572359



Internal ID16359768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34960264hg38UCSC Ensembl
Innerchr16:34173678..34194635hg19UCSC Ensembl
Innerchr16:34031179..34052136hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820981
hg1920958
hg1820958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856207, nssv856205, nssv856206
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572359
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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