A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067307



Internal ID18809838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81798426..81818131hg38UCSC Ensembl
Innerchr16:81832031..81851736hg19UCSC Ensembl
Innerchr16:80389532..80409237hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3819706
hg1919706
hg1819706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719083
Samples
Known GenesPLCG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067307
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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