A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571621



Internal ID16359030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20538778..20553068hg38UCSC Ensembl
Innerchr16:20550100..20564390hg19UCSC Ensembl
Innerchr16:20457601..20471891hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3814291
hg1914291
hg1814291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv853080
Samples
Known GenesACSM2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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