A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572556



Internal ID16359965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48470453..48476844hg38UCSC Ensembl
Innerchr16:48504364..48510755hg19UCSC Ensembl
Innerchr16:47061865..47068256hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg386392
hg196392
hg186392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856691
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572556
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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