A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049471



Internal ID19138690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934316..19959531hg38UCSC Ensembl
Innerchr16:19945638..19970853hg19UCSC Ensembl
Innerchr16:19853139..19878354hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3825216
hg1925216
hg1825216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3546899, nssv3546897, nssv3546898, nssv3546896, nssv3546900
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)nsv1049471
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer