A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572881



Internal ID16360290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63042506..63085645hg38UCSC Ensembl
Innerchr16:63076410..63119549hg19UCSC Ensembl
Innerchr16:61633911..61677050hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3843140
hg1943140
hg1843140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5176n54
Supporting Variantsnssv859055
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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