A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859056



Internal ID16153012
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 StatusS
Merged Variantsnsv572882
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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