A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3542784



Internal ID18841065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19931704..19954015hg38UCSC Ensembl
Innerchr16:19943026..19965337hg19UCSC Ensembl
Innerchr16:19850527..19872838hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3822312
hg1922312
hg1822312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046426
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3542784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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