A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1891725



Internal ID17417289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61795767..61796411hg38UCSC Ensembl
Innerchr11:61563239..61563883hg19UCSC Ensembl
Innerchr11:61319815..61320459hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975935
Supporting Variants
SamplesHGDP00542
Known GenesFEN1
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)nssv1891725
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer