A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065088



Internal ID19154307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81844876..81919643hg38UCSC Ensembl
Innerchr16:81878481..81953248hg19UCSC Ensembl
Innerchr16:80435982..80510749hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3874768
hg1974768
hg1874768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559840, nssv3559839
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)nsv1065088
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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