A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719083



Internal ID18670678
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 StatusS
Merged Variantsnsv1067307
Supporting Variants
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)nssv3719083
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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