A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042868



Internal ID19132087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:881686..966057hg38UCSC Ensembl
Innerchr16:931686..1016057hg19UCSC Ensembl
Innerchr16:871687..956058hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3884372
hg1984372
hg1884372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718827
Samples
Known GenesLMF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042868
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