A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573302



Internal ID16360711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80791309..80824246hg38UCSC Ensembl
Innerchr16:80825206..80858143hg19UCSC Ensembl
Innerchr16:79382707..79415644hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3832938
hg1932938
hg1832938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149307
Samples1780862415_A
Known GenesCDYL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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