A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522140



Internal ID15449433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81475688..81477137hg38UCSC Ensembl
Innerchr16:81509293..81510742hg19UCSC Ensembl
Innerchr16:80066794..80068243hg18UCSC Ensembl
Innerchr16:80066794..80068243hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg381450
hg191450
hg181450
hg171450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694135
Samples
Known GenesCMIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522140
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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