A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559309



Internal ID18857590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55756974..55795666hg38UCSC Ensembl
Innerchr16:55790886..55829578hg19UCSC Ensembl
Innerchr16:54348387..54387079hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3838693
hg1938693
hg1838693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066137
Supporting Variants
Samples
Known GenesCES1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559309
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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