A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699460



Internal ID15089426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57972365..57990436hg38UCSC Ensembl
Innerchr16:58006269..58024340hg19UCSC Ensembl
Innerchr16:56563770..56581841hg18UCSC Ensembl
Innerchr16:56563770..56581841hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3818072
hg1918072
hg1818072
hg1718072
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523659
Supporting Variants
Samples
Known GenesTEPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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