A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063660



Internal ID18806191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46896711..46944880hg38UCSC Ensembl
Innerchr16:46930623..46978792hg19UCSC Ensembl
Innerchr16:45488124..45536293hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3848170
hg1948170
hg1848170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559244
Samples
Known GenesGPT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063660
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