A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571021



Internal ID16358430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:696914..725505hg38UCSC Ensembl
Innerchr16:746914..775505hg19UCSC Ensembl
Innerchr16:686915..715506hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3828592
hg1928592
hg1828592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851746
Samples
Known GenesCCDC78, FAM173A, FBXL16, METRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571021
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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