A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046472



Internal ID19135691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19932666..19959531hg38UCSC Ensembl
Innerchr16:19943988..19970853hg19UCSC Ensembl
Innerchr16:19851489..19878354hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3826866
hg1926866
hg1826866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3542855
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)nsv1046472
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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