A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857481



Internal ID16151437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:54379818..54409311hg38UCSC Ensembl
Innerchr16:54413730..54443223hg19UCSC Ensembl
Innerchr16:52971231..53000724hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3829494
hg1929494
hg1829494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572627
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)nssv857481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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