A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1959509



Internal ID17811414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35309558..35310518hg38UCSC Ensembl
Innerchr13:35883695..35884655hg19UCSC Ensembl
Innerchr13:34781695..34782655hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38961
hg19961
hg18961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv974080
Supporting Variants
SamplesHGDP00927
Known GenesNBEA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1959509
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