A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050237



Internal ID18792768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4641028..4744872hg38UCSC Ensembl
Innerchr16:4691029..4794873hg19UCSC Ensembl
Innerchr16:4631030..4734874hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38103845
hg19103845
hg18103845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556973
Samples
Known GenesANKS3, C16orf71, MGRN1, MIR6769A, NUDT16L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050237
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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