A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155361



Internal ID22085866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83665118..84451429hg38UCSC Ensembl
Outerchr16:83665101..84461124hg38UCSC Ensembl
Innerchr16:83698723..84485035hg19UCSC Ensembl
Outerchr16:83698706..84494730hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38796024
hg19796025
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009955
Samples
Known GenesADAD2, ATP2C2, CDH13, DNAAF1, HSBP1, HSDL1, KCNG4, MBTPS1, MLYCD, NECAB2, OSGIN1, SLC38A8, TAF1C, WFDC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155361
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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