A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155379



Internal ID22085884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15639847..15643476hg38UCSC Ensembl
Outerchr17:15623842..15650964hg38UCSC Ensembl
Innerchr17:15543161..15546790hg19UCSC Ensembl
Outerchr17:15527156..15554278hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3827123
hg1927123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010108, nssv4010105, nssv4010103, nssv4010104, nssv4010106
Samples
Known GenesTRIM16
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155379
Frequency
Sample Size131
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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