A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066499



Internal ID18809030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89891957..90028891hg38UCSC Ensembl
Innerchr16:89958365..90095299hg19UCSC Ensembl
Innerchr16:88485866..88622800hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38136935
hg19136935
hg18136935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560010
Samples
Known GenesAFG3L1P, CENPBD1, DBNDD1, DEF8, GAS8, MC1R, TCF25, TUBB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066499
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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