A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572882



Internal ID16360291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63043867..63069105hg38UCSC Ensembl
Innerchr16:63077771..63103009hg19UCSC Ensembl
Innerchr16:61635272..61660510hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3825239
hg1925239
hg1825239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859056
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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