A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656208



Internal ID15046174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1757779..1764439hg38UCSC Ensembl
Innerchr16:1807780..1814440hg19UCSC Ensembl
Innerchr16:1747781..1754441hg18UCSC Ensembl
Innerchr16:1747781..1754441hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386661
hg196661
hg186661
hg176661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517196
Supporting Variants
Samples
Known GenesMAPK8IP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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