A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1896294



Internal ID17872250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75704125..75707513hg38UCSC Ensembl
Innerchr11:75415170..75418558hg19UCSC Ensembl
Innerchr11:75092818..75096206hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383389
hg193389
hg183389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983044
Supporting Variants
SamplesHGDP01284
Known Genes
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)nssv1896294
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