A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559959



Internal ID18858240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84582619..84612845hg38UCSC Ensembl
Innerchr16:84616225..84646451hg19UCSC Ensembl
Innerchr16:83173726..83203952hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3830227
hg1930227
hg1830227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062836
Supporting Variants
Samples
Known GenesCOTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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