A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060404



Internal ID18802935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69954471..70091259hg38UCSC Ensembl
Innerchr16:69988374..70125162hg19UCSC Ensembl
Innerchr16:68545875..68682663hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38136789
hg19136789
hg18136789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2999n100
Supporting Variantsnssv3559449, nssv3559448
Samples
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060404
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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