A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054779



Internal ID18797310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8443804..8558535hg38UCSC Ensembl
Innerchr16:8493806..8608537hg19UCSC Ensembl
Innerchr16:8433807..8548538hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38114732
hg19114732
hg18114732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718868
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054779
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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