A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572836



Internal ID16360245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60788213..61285302hg38UCSC Ensembl
Innerchr16:60822117..61319206hg19UCSC Ensembl
Innerchr16:59379618..59876707hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38497090
hg19497090
hg18497090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858908
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572836
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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