A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572628



Internal ID16360037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:54380531..54385662hg38UCSC Ensembl
Innerchr16:54414443..54419574hg19UCSC Ensembl
Innerchr16:52971944..52977075hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg385132
hg195132
hg185132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5124n54
Supporting Variantsnssv857482
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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