A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572901



Internal ID16013624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64930330..64956284hg38UCSC Ensembl
Innerchr16:64964233..64990187hg19UCSC Ensembl
Innerchr16:63521734..63547688hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3825955
hg1925955
hg1825955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859068
Samples
Known GenesCDH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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