A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061544



Internal ID18804075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81800708..81843770hg38UCSC Ensembl
Innerchr16:81834313..81877375hg19UCSC Ensembl
Innerchr16:80391814..80434876hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3843063
hg1943063
hg1843063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559838
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)nsv1061544
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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