A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155330



Internal ID22085835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990686..70179141hg38UCSC Ensembl
Outerchr16:69954483..70200633hg38UCSC Ensembl
Innerchr16:70024589..70213044hg19UCSC Ensembl
Outerchr16:69988386..70234536hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38246151
hg19246151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008819
Samples
Known GenesCLEC18A, CLEC18C, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155330
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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