A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1881324



Internal ID17867944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33189060..33190527hg38UCSC Ensembl
Innerchr11:33210606..33212073hg19UCSC Ensembl
Innerchr11:33167182..33168649hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381468
hg191468
hg181468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971999
Supporting Variants
SamplesHGDP01284
Known GenesCSTF3-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1881324
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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