A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525861



Internal ID15106468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1853650..1858255hg38UCSC Ensembl
Innerchr16:1903651..1908256hg19UCSC Ensembl
Innerchr16:1843652..1848257hg18UCSC Ensembl
Innerchr16:1843652..1848257hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384606
hg194606
hg184606
hg174606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702057
Samples
Known GenesMEIOB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525861
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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