A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037982



Internal ID18780513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..136739hg38UCSC Ensembl
Innerchr16:60765..186738hg19UCSC Ensembl
Innerchr16:765..126738hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38125975
hg19125974
hg18125974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2689n100
Supporting Variantsnssv3556935
Samples
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, MPG, NPRL3, POLR3K, RHBDF1, SNRNP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037982
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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