A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064951



Internal ID18807482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70117612..70212503hg38UCSC Ensembl
Innerchr16:70151515..70246406hg19UCSC Ensembl
Innerchr16:68709016..68803907hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3894892
hg1994892
hg1894892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3012n100
Supporting Variantsnssv3559532
Samples
Known GenesCLEC18C, PDPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064951
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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