A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521726



Internal ID15449019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56331443..56353557hg38UCSC Ensembl
Innerchr16:56365355..56387469hg19UCSC Ensembl
Innerchr16:54922856..54944970hg18UCSC Ensembl
Innerchr16:54922856..54944970hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3822115
hg1922115
hg1822115
hg1722115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694486
Samples
Known GenesGNAO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521726
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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