A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570986



Internal ID16358395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:525312..546762hg38UCSC Ensembl
Innerchr16:575312..596762hg19UCSC Ensembl
Innerchr16:515313..536763hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3821451
hg1921451
hg1821451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851701
Samples
Known GenesCAPN15, LINC00235, MIR3176, MIR5587
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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