A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2982n100



Internal ID20154598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55507884..55555666hg38UCSC Ensembl
chr16:55541796..55589578hg19UCSC Ensembl
chr16:54099297..54147079hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3847783
hg1947783
hg1847783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056858, nsv1064647, nsv1061647, nsv1067520, nsv1062896, nsv1056211
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)dgv2982n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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