A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573387



Internal ID16014110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83069628..83115320hg38UCSC Ensembl
Innerchr16:83103233..83148925hg19UCSC Ensembl
Innerchr16:81660734..81706426hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3845693
hg1945693
hg1845693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861966
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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