A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063684



Internal ID18806215
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 StatusM
Merged Variantsdgv2983n100
Supporting Variantsnssv3559276
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)nsv1063684
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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