A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702543



Internal ID15092509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83940461..83971648hg38UCSC Ensembl
Innerchr16:83974066..84005253hg19UCSC Ensembl
Innerchr16:82531567..82562754hg18UCSC Ensembl
Innerchr16:82531567..82562754hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3831188
hg1931188
hg1831188
hg1731188
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517566
Supporting Variants
Samples
Known GenesNECAB2, OSGIN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702543
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