A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571665



Internal ID16359074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22701658..22777529hg38UCSC Ensembl
Innerchr16:22712979..22788850hg19UCSC Ensembl
Innerchr16:22620480..22696351hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3875872
hg1975872
hg1875872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv853137
Samples
Known GenesMIR548AA2, MIR548D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571665
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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