A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067520



Internal ID18810051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55514410..55555666hg38UCSC Ensembl
Innerchr16:55548322..55589578hg19UCSC Ensembl
Innerchr16:54105823..54147079hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3841257
hg1941257
hg1841257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2982n100
Supporting Variantsnssv3559284
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)nsv1067520
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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