A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055556



Internal ID19144775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80903546..80920979hg38UCSC Ensembl
Innerchr16:80937443..80954876hg19UCSC Ensembl
Innerchr16:79494944..79512377hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3817434
hg1917434
hg1817434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3045n100
Supporting Variantsnssv3559792
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)nsv1055556
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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