A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525138



Internal ID15452431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9623512..9690306hg38UCSC Ensembl
Innerchr16:9717369..9784163hg19UCSC Ensembl
Innerchr16:9624870..9691664hg18UCSC Ensembl
Innerchr16:9624870..9691664hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3866795
hg1966795
hg1866795
hg1766795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv162n21
Supporting Variantsnssv701208
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525138
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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