A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066766



Internal ID18809297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55514410..55542249hg38UCSC Ensembl
Innerchr16:55548322..55576161hg19UCSC Ensembl
Innerchr16:54105823..54133662hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3827840
hg1927840
hg1827840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2983n100
Supporting Variantsnssv3559277, nssv3559279, nssv3559278
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)nsv1066766
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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