A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155364



Internal ID22085869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86240009..86258687hg38UCSC Ensembl
Outerchr16:86232426..86268426hg38UCSC Ensembl
Innerchr16:86273615..86292293hg19UCSC Ensembl
Outerchr16:86266032..86302032hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3836001
hg1936001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009987, nssv4009988, nssv4009985
Samples
Known GenesLINC01081
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155364
Frequency
Sample Size131
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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