A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704986



Internal ID15094952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83937637..84050522hg38UCSC Ensembl
Innerchr16:83971242..84084127hg19UCSC Ensembl
Innerchr16:82528743..82641628hg18UCSC Ensembl
Innerchr16:82528743..82641628hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38112886
hg19112886
hg18112886
hg17112886
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528396
Supporting Variants
Samples
Known GenesNECAB2, OSGIN1, SLC38A8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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