A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062896



Internal ID18805427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55514410..55551969hg38UCSC Ensembl
Innerchr16:55548322..55585881hg19UCSC Ensembl
Innerchr16:54105823..54143382hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3837560
hg1937560
hg1837560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2982n100
Supporting Variantsnssv3559283, nssv3559282
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)nsv1062896
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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