A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013659



Internal ID22075290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50059963..50090736hg38UCSC Ensembl
Outerchr19:50055880..50135241hg38UCSC Ensembl
Innerchr19:50563220..50593993hg19UCSC Ensembl
Outerchr19:50559137..50638498hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3879362
hg1979362
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155602
Supporting Variants
Samples
Known GenesFLJ26850, SNAR-A10, SNAR-A11, SNAR-A14, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-B1, SNAR-B2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013659
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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