A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053617



Internal ID18796148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12637101..12777782hg38UCSC Ensembl
Innerchr16:12730958..12871639hg19UCSC Ensembl
Innerchr16:12638459..12779140hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38140682
hg19140682
hg18140682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718885
Samples
Known GenesCPPED1, MIR4718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053617
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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