A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703937



Internal ID15440589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84030777..84050522hg38UCSC Ensembl
Innerchr16:84064382..84084127hg19UCSC Ensembl
Innerchr16:82621883..82641628hg18UCSC Ensembl
Innerchr16:82621883..82641628hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3819746
hg1919746
hg1819746
hg1719746
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527489
Supporting Variants
Samples
Known GenesSLC38A8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703937
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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