A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155350



Internal ID22085855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77013263..77076598hg38UCSC Ensembl
Outerchr16:77010008..77077378hg38UCSC Ensembl
Innerchr16:77047160..77110495hg19UCSC Ensembl
Outerchr16:77043905..77111275hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3867371
hg1967371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009885
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155350
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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