A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516716



Internal ID15097323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10565039..10566029hg38UCSC Ensembl
Innerchr16:10658896..10659886hg19UCSC Ensembl
Innerchr16:10566397..10567387hg18UCSC Ensembl
Innerchr16:10566397..10567387hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38991
hg19991
hg18991
hg17991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670815, nssv670388, nssv671190, nssv680429, nssv681036, nssv693033, nssv676903, nssv682923, nssv690675
Samples
Known GenesEMP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516716
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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