A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044119



Internal ID19133338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19934316..19964959hg38UCSC Ensembl
Innerchr16:19945638..19976281hg19UCSC Ensembl
Innerchr16:19853139..19883782hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3830644
hg1930644
hg1830644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2791n100
Supporting Variantsnssv3546956
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)nsv1044119
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