A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522890



Internal ID15450183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81307758..81314791hg38UCSC Ensembl
Innerchr16:81341363..81348396hg19UCSC Ensembl
Innerchr16:79898864..79905897hg18UCSC Ensembl
Innerchr16:79898864..79905897hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg387034
hg197034
hg187034
hg177034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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