A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559276



Internal ID18510871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55514410..55538973hg38UCSC Ensembl
Innerchr16:55548322..55572885hg19UCSC Ensembl
Innerchr16:54105823..54130386hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3824564
hg1924564
hg1824564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063684
Supporting Variants
Samples
Known GenesLPCAT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559276
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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